Changes between Version 1 and Version 2 of UTGBManual


Ignore:
Timestamp:
08/15/07 15:20:52 (18 years ago)
Author:
leo
Comment:

--

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  • UTGBManual

    v1 v2  
    11= UTGB Manual =
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     126
     127</head>
     128
     129<body lang=JA link=blue vlink=purple style='text-justify-trim:punctuation'>
     130
     131<div class=Section1 style='layout-grid:18.0pt'>
     132
     133<h1 align=center style='text-align:center'><span lang=EN-US style='font-size:
     13424.0pt'>&nbsp;</span></h1>
     135
     136<h1 align=center style='text-align:center'><span lang=EN-US style='font-size:
     13724.0pt'>&nbsp;</span></h1>
     138
     139<h1 align=center style='text-align:center'><span lang=EN-US style='font-size:
     14036.0pt'>UT Genome Browser</span></h1>
     141
     142<h1 align=center style='text-align:center'><span lang=EN-US style='font-size:
     14336.0pt'>&nbsp;</span></h1>
     144
     145<h1 align=center style='text-align:center'><span lang=EN-US style='font-size:
     14636.0pt'>User’s Manual</span></h1>
     147
     148<h1 align=center style='text-align:center'><span lang=EN-US style='font-size:
     14936.0pt'>Version 1.0</span></h1>
     150
     151<h1 align=center style='text-align:center'><span lang=EN-US style='font-size:
     15224.0pt'>&nbsp;</span></h1>
     153
     154<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     155
     156<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     157
     158<p class=MsoNormal align=center style='text-align:center'><b><span
     159 lang=EN-US style='font-size:24.0pt'>August 17, 2004</span></b></p>
     160
     161<h1 align=center style='text-align:center'><span lang=EN-US style='font-size:
     16224.0pt'>&nbsp;</span></h1>
     163
     164<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     165
     166<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     167
     168<h1 align=center style='text-align:center'><span lang=EN-US style='font-size:
     16922.0pt'>UT Genome Browser Development Team</span></h1>
     170
     171<h1 align=center style='text-align:center'><span lang=EN-US style='font-size:
     17222.0pt'>&nbsp;</span></h1>
     173
     174<b><span lang=EN-US style='font-size:18.0pt;font-family:Century'><br clear=all
     175style='page-break-before:always'>
     176</span></b>
     177
     178<h1><span lang=EN-US>Table of Contents</span></h1>
     179
     180<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     181
     182<p class=MsoNormal style='margin-left:21.25pt;text-indent:-21.25pt;line-height:
     183150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>1<span
     184style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     185</span></span></b><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>Welcome</span></b></p>
     186
     187<p class=MsoNormal style='margin-left:21.25pt;text-indent:-21.25pt;line-height:
     188150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>2<span
     189style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     190</span></span></b><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>Keyword
     191Search</span></b></p>
     192
     193<p class=MsoNormal style='margin-left:49.6pt;text-indent:-10.0mm;line-height:
     194150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>2.1<span
     195style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp; </span></span></b><b><span
     196lang=EN-US style='font-size:14.0pt;line-height:150%'>Gene List</span></b></p>
     197
     198<p class=MsoNormal style='margin-left:49.6pt;text-indent:-10.0mm;line-height:
     199150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>2.2<span
     200style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp; </span></span></b><b><span
     201lang=EN-US style='font-size:14.0pt;line-height:150%'>Mapping Position List</span></b></p>
     202
     203<p class=MsoNormal style='margin-left:21.25pt;text-indent:-21.25pt;line-height:
     204150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>3<span
     205style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     206</span></span></b><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>Online
     207Sequence Alignment</span></b></p>
     208
     209<p class=MsoNormal style='margin-left:21.25pt;text-indent:-21.25pt;line-height:
     210150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>4<span
     211style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     212
     213</span></span></b><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>Main
     214Window</span></b></p>
     215
     216<p class=MsoNormal style='margin-left:49.6pt;text-indent:-10.0mm;line-height:
     217150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>4.1<span
     218style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp; </span></span></b><b><span
     219lang=EN-US style='font-size:14.0pt;line-height:150%'>Scrolling and Zooming the
     220Main Window</span></b></p>
     221
     222<p class=MsoNormal style='margin-left:49.6pt;text-indent:-10.0mm;line-height:
     223150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>4.2<span
     224style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp; </span></span></b><b><span
     225lang=EN-US style='font-size:14.0pt;line-height:150%'>Functions of Buttons</span></b></p>
     226
     227<p class=MsoNormal style='margin-left:49.6pt;text-indent:-10.0mm;line-height:
     228150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>4.3<span
     229style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp; </span></span></b><b><span
     230lang=EN-US style='font-size:14.0pt;line-height:150%'>Addition, Deletion, and
     231Rearrangement of Tracks</span></b></p>
     232
     233<p class=MsoNormal style='margin-left:49.6pt;text-indent:-10.0mm;line-height:
     234150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>4.4<span
     235style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp; </span></span></b><b><span
     236lang=EN-US style='font-size:14.0pt;line-height:150%'>Setting for Tracks</span></b></p>
     237
     238<p class=MsoNormal style='margin-left:21.25pt;text-indent:-21.25pt;line-height:
     239150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>5<span
     240style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     241</span></span></b><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>Pre-defined
     242Tracks</span></b></p>
     243
     244<p class=MsoNormal style='margin-left:49.6pt;text-indent:-10.0mm;line-height:
     245150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>5.1<span
     246style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp; </span></span></b><b><span
     247lang=EN-US style='font-size:14.0pt;line-height:150%'>Overview Tracks</span></b></p>
     248
     249<p class=MsoNormal style='margin-left:49.6pt;text-indent:-10.0mm;line-height:
     250150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>5.2<span
     251style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp; </span></span></b><b><span
     252lang=EN-US style='font-size:14.0pt;line-height:150%'>Ruler and Zooming Tracks</span></b></p>
     253
     254<p class=MsoNormal style='margin-left:49.6pt;text-indent:-10.0mm;line-height:
     255150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>5.3<span
     256style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp; </span></span></b><b><span
     257lang=EN-US style='font-size:14.0pt;line-height:150%'>Base Color Track</span></b></p>
     258
     259<p class=MsoNormal style='margin-left:49.6pt;text-indent:-10.0mm;line-height:
     260150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>5.4<span
     261style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp; </span></span></b><b><span
     262lang=EN-US style='font-size:14.0pt;line-height:150%'>Gap Track</span></b></p>
     263
     264<p class=MsoNormal style='margin-left:49.6pt;text-indent:-10.0mm;line-height:
     265150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>5.5<span
     266style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp; </span></span></b><b><span
     267lang=EN-US style='font-size:14.0pt;line-height:150%'>GC Content Track</span></b></p>
     268
     269<p class=MsoNormal style='margin-left:49.6pt;text-indent:-10.0mm;line-height:
     270150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>5.6<span
     271style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp; </span></span></b><b><span
     272lang=EN-US style='font-size:14.0pt;line-height:150%'>Mapped Gene Track</span></b></p>
     273
     274<p class=MsoNormal style='margin-left:49.6pt;text-indent:-10.0mm;line-height:
     275150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>5.7<span
     276style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp; </span></span></b><b><span
     277lang=EN-US style='font-size:14.0pt;line-height:150%'>Genscan Track</span></b></p>
     278
     279<p class=MsoNormal style='margin-left:49.6pt;text-indent:-10.0mm;line-height:
     280150%'><b><span lang=EN-US style='font-size:14.0pt;line-height:150%'>5.8<span
     281style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp; </span></span></b><b><span
     282lang=EN-US style='font-size:14.0pt;line-height:150%'>Comparative Genomics Track</span></b></p>
     283
     284<p class=MsoNormal style='line-height:150%'><b><span lang=EN-US
     285style='font-size:14.0pt;line-height:150%'>Ramen Assembler / UT Genome Browser
     286Team Members</span></b></p>
     287
     288<p class=MsoNormal style='line-height:150%'><b><span lang=EN-US
     289style='font-size:14.0pt;line-height:150%'>Acknowledgements</span></b></p>
     290
     291<span lang=EN-US style='font-size:10.5pt;line-height:150%;font-family:Century'><br
     292clear=all style='page-break-before:always'>
     293</span>
     294
     295<p class=MsoNormal style='line-height:150%'><span class=a><span lang=EN-US
     296style='font-size:18.0pt;line-height:150%'>1. Welcome</span></span></p>
     297
     298<p class=MsoNormal><span lang=EN-US>Welcome to UT Genome Browser (University of Tokyo Genome Browser). With this browser you can browse genomic information
     299of a target species (at present Medaka only) from several aspects. For example,
     300the following tasks can be performed with different combinations. </span></p>
     301
     302<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     303lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     304</span></span><span lang=EN-US>You can search gene, by gene name, clone name,
     305cluster name and display its surroundings gene groups.</span></p>
     306
     307<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     308lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     309</span></span><span lang=EN-US>You can map a genomic sequence to any genome and
     310observe its surroundings.</span></p>
     311
     312<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     313lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     314</span></span><span lang=EN-US>You can save the sequence itself on your system
     315from here.</span></p>
     316
     317<p class=MsoNormal><span lang=EN-US>Questions, suggestions or comments are
     318welcome to <a href="mailto:webmaster@utgenome.org">webmaster@utgenome.org</a>.</span></p>
     319
     320<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     321
     322<h1><span lang=EN-US>2. Keyword Search </span></h1>
     323
     324<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     325border=0 width=254 height=262 src="manual_e.files/image001.jpg"
     326alt="keyword_top.png"></span></p>
     327
     328<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     329
     330<p class=MsoNormal><span lang=EN-US>The top window displays the keyword search
     331engine, as above picture illustrates. Inputting any keyword at the query box, we
     332can see the detail information about the query. More about keyword search can
     333be found in the help, written on the same window. In addition, if the keyword
     334is a part of targets, then all the targets will be displayed. For example, the
     335keyword “BCD” will match to “ABCD”, “BCDE”, “BCD” and “BCDF” etc. (this is
     336worked out with using a suffix array.)</span></p>
     337
     338<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     339
     340<h2><span lang=EN-US>2.1. Gene List</span></h2>
     341
     342<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     343border=0 width=288 height=235 src="manual_e.files/image002.jpg"
     344alt="keyword_genes.png"></span></p>
     345
     346<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     347
     348<p class=MsoNormal><span lang=EN-US>When there are many genes for one keyword
     349search, all genes will be displayed on a list. Pressing the (*) button on the
     350left side, you can go to the mapped region for the gene. This list appears when
     351multiple candidate entries are found, typically when class names or part of a
     352gene number are input as a keyword. If a Genebank accession number is given,
     353the number must be unique, and hence this list does not appear.&nbsp; </span></p>
     354
     355<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     356
     357<h2><span lang=EN-US>2.2. Mapping Position List</span></h2>
     358
     359<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     360border=0 width=384 height=230 src="manual_e.files/image003.jpg"
     361alt="keyword_locs.png"></span></p>
     362
     363<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     364
     365<p class=MsoNormal><span lang=EN-US>If the query gene has mapped to several
     366regions on the genomic sequence, the list of all positions will be shown. Pressing
     367the (*) button on the left side displays the mapped region of the gene. If
     368there is only one mapped region of the gene, the list is skipped to display.</span></p>
     369
     370<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     371
     372<h1><span lang=EN-US>3. Sequence Alignment </span></h1>
     373
     374<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     375border=0 width=408 height=195 src="manual_e.files/image004.jpg"
     376alt=online01.PNG></span></p>
     377
     378<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     379
     380<p class=MsoNormal><span lang=EN-US>Sequence mapping is possible by inputting a
     381sequence in the online mapping frame (above image) at the bottom of the main
     382window. After selecting the species and its revision, press the search button
     383on the bottom. The request is sent to the alignment server ALPS to align the
     384given sequence to the selected genome. Afterwards, the list of alignment
     385results is returned if the system finds some alignments.</span></p>
     386
     387<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     388border=0 width=353 height=431 src="manual_e.files/image005.jpg"></span></p>
     389
     390<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     391
     392<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     393border=0 width=400 height=81 src="manual_e.files/image006.jpg"
     394alt=online02.PNG></span></p>
     395
     396<p class=MsoNormal><span lang=EN-US>From the list, you can select one alignment
     397by clicking the result button as illustrated above. Then, the aligned result
     398will appear on the browser. The ALPS mapping track in following snapshot
     399displays the added mapping status.</span></p>
     400
     401<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     402
     403<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     404border=0 width=566 height=149 src="manual_e.files/image007.jpg"
     405alt=online03.PNG></span></p>
     406
     407<h1><span lang=EN-US>4. Main Window</span></h1>
     408
     409<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     410border=0 width=509 height=324 src="manual_e.files/image008.jpg"
     411alt="browser_main.png"></span></p>
     412
     413<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     414
     415<p class=MsoNormal><span lang=EN-US>The above picture shows the main screen for
     416UT Genome Browser. It is possible to see the targeted region of genomic
     417sequence by many tracks. This browser provides the following functions to
     418manipulate tracks on this image screen.</span></p>
     419
     420<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     421lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     422</span></span><span lang=EN-US>Shifting, zooming in and out, and reversing of
     423the target region. It facilitates zooming in the sequence until bases can be
     424seen, while providing a panoramic, structural view for the sequence.</span></p>
     425
     426<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     427lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     428</span></span><span lang=EN-US>Adding, deleting and reordering the tracks.</span></p>
     429
     430<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     431lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     432</span></span><span lang=EN-US>Customizing of each track’s display.</span></p>
     433
     434<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     435lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     436</span></span><span lang=EN-US>Retrieving the present displayed sequence in Fasta
     437format.</span></p>
     438
     439<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     440lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     441</span></span><span lang=EN-US>Continuing keyword search.</span></p>
     442
     443<p class=MsoNormal><span lang=EN-US>In what follows, we describe the detail
     444about each function.</span></p>
     445
     446<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     447
     448<h2><span lang=EN-US>4.1&nbsp;&nbsp; Scrolling and zooming the main window </span></h2>
     449
     450<p class=MsoNormal><span lang=EN-US>On main window, it is possible to shift and
     451to zoom in/out the present observing sequence. These tasks can be carried out
     452by:</span></p>
     453
     454<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     455lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     456</span></span><span lang=EN-US>Inputting value in the input box method.</span></p>
     457
     458<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     459lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     460</span></span><span lang=EN-US>Using shifting button method.</span></p>
     461
     462<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     463lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     464</span></span><span lang=EN-US>Using overview, ruler and zooming track method.</span></p>
     465
     466<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     467
     468<h3 style='text-align:justify;text-justify:inter-ideograph'><span lang=EN-US>Inputting
     469value in the input box method</span></h3>
     470
     471<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     472border=0 width=552 height=31 src="manual_e.files/image009.jpg"
     473alt="browser_params.png"></span></p>
     474
     475<p class=MsoNormal><span lang=EN-US>You can input values into the input boxes
     476(like above image) inside the main window. The details about this method are as
     477follows,</span></p>
     478
     479<p class=MsoNormal style='margin-left:31.5pt;text-indent:-21.0pt'><span
     480lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     481</span></span><b><span lang=EN-US>Species: </span></b><span lang=EN-US>Select
     482the species to display. The selectable revisions would be changed with respect
     483to the species. At present, only Medaka is possible to be selected.</span></p>
     484
     485<p class=MsoNormal style='margin-left:31.5pt;text-indent:-21.0pt'><span
     486lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     487</span></span><b><span lang=EN-US>Revision</span></b><span lang=EN-US>: Select
     488the revision of the target specie’s genome. For Medaka, the revision name
     489format is yyyymm. The selecting topics will change with respect to the selected
     490revision.</span></p>
     491
     492<p class=MsoNormal style='margin-left:31.5pt;text-indent:-21.0pt'><span
     493lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     494</span></span><b><span lang=EN-US>Target: </span></b><span lang=EN-US>Select
     495the target region to be displayed, from the selected species and selected
     496revision. In the case of 200406 revision of Medaka, only scaffold name (e.g.
     497scaffold123) can be selected but not the chromosome name (e.g. chr10). Chromosome
     498numbers will be available in our later revision. </span></p>
     499
     500<p class=MsoNormal style='margin-left:31.5pt;text-indent:-21.0pt'><span
     501lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     502</span></span><b><span lang=EN-US>Start: </span></b><span lang=EN-US>Select the
     503start position from your targeted sequence to display. The number should be 1-origin
     504(i.e. the starting point will be 1).</span></p>
     505
     506<p class=MsoNormal style='margin-left:31.5pt;text-indent:-21.0pt'><span
     507lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     508
     509</span></span><b><span lang=EN-US>End: </span></b><span lang=EN-US>Select the
     510end point from your targeted sequence to display. The number should be 1-origin.
     511If the ending point is greater than the starting point then the display will be
     512normal. Otherwise, the display will be reverse. In both cases, the ending base
     513will be included in the displaying sequence.</span></p>
     514
     515<p class=MsoNormal style='margin-left:31.5pt;text-indent:-21.0pt'><span
     516lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     517</span></span><b><span lang=EN-US>Width: </span></b><span lang=EN-US>Input the
     518width in terms of pixels for output track display. Input the value that is
     519suitable for your vision. Normally, it is assumed that width is equal to the
     520screen width. It is also possible to input the width as 10 times bigger than
     521the screen width. In that case, it seems to be convenient to use the scroll of
     522the browser.</span></p>
     523
     524<p class=MsoNormal><span lang=EN-US>After manipulating the previous items,
     525press the “Apply” button to shifting to the desired position of the sequence.</span></p>
     526
     527<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     528
     529<h3 style='text-align:justify;text-justify:inter-ideograph'><span lang=EN-US>Using
     530shifting button method</span></h3>
     531
     532<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     533border=0 width=267 height=25 src="manual_e.files/image010.jpg"
     534alt="browser_moves.png"></span></p>
     535
     536<p class=MsoNormal><span lang=EN-US>Moreover, there is another method by using
     537the button (like above image). Normally, the input box method is useful only when
     538it is important to have the correct position of the sequence.&nbsp; As number
     539must be supplied in this method, sometime this process is quit cumbersome. So
     540we provide more intuitive methods for your convenience. So the buttons related
     541to these methods are as follows,</span></p>
     542
     543<p class=MsoNormal style='margin-left:31.5pt;text-indent:-21.0pt'><span
     544lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     545</span></span><b><span lang=EN-US>Shifting (</span></b><span lang=EN-US><img
     546border=0 width=18 height=13 src="manual_e.files/image011.jpg" alt=rr.png><b>,</b><img
     547border=0 width=13 height=13 src="manual_e.files/image012.jpg" alt=r.png><b>,</b><img
     548border=0 width=13 height=13 src="manual_e.files/image013.jpg" alt=f.png><b>,</b><img
     549border=0 width=18 height=13 src="manual_e.files/image014.jpg" alt=ff.png><b>):&nbsp;
     550</b><img border=0 width=18 height=13 src="manual_e.files/image011.jpg"
     551alt=rr.png><b>,</b><img border=0 width=13 height=13
     552src="manual_e.files/image012.jpg" alt=r.png><b>,</b><img border=0 width=13
     553height=13 src="manual_e.files/image013.jpg" alt=f.png><b>,</b><img border=0
     554width=18 height=13 src="manual_e.files/image015.jpg" alt=ff.png> are buttons to
     555shifting the sequence. The<img border=0 width=18 height=13
     556src="manual_e.files/image011.jpg" alt=rr.png> button scrolls sequence up to one
     557screen size where the <img border=0 width=13 height=13
     558src="manual_e.files/image012.jpg" alt=r.png>&nbsp;button scrolls half screen to
     559the left. The inverse buttons are for shifting to the right.&nbsp;&nbsp; </span></p>
     560
     561<p class=MsoNormal style='margin-left:31.5pt;text-indent:-21.0pt'><span
     562lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     563</span></span><b><span lang=EN-US>Scaling (<img border=0 width=13 height=13
     564src="manual_e.files/image016.jpg" alt=zoomout.png>, <img border=0 width=13
     565height=13 src="manual_e.files/image017.jpg" alt=zoomin.png>, <img border=0
     566width=18 height=13 src="manual_e.files/image018.jpg" alt=zoom10x.png>, <img
     567border=0 width=18 height=13 src="manual_e.files/image019.jpg" alt=zoom1x.png>, <img
     568border=0 width=18 height=13 src="manual_e.files/image020.jpg" alt=zoom01x.png>,
     569<img border=0 width=18 height=13 src="manual_e.files/image021.jpg"
     570alt=zoom001x.png>, <img border=0 width=18 height=13
     571src="manual_e.files/image022.jpg" alt=zoom0001x.png>):&nbsp; </span></b><span
     572lang=EN-US>The <b><img border=0 width=13 height=13
     573src="manual_e.files/image016.jpg" alt=zoomout.png></b>&nbsp;button does scaling
     574down and the display will be half of the present size where <b><img border=0
     575width=13 height=13 src="manual_e.files/image017.jpg" alt=zoomin.png></b>&nbsp;button
     576does scaling up and the display will be 2 times bigger than present size. The
     577fractional form button specifies the scale directly. The scaling unit is
     5781bp/pixel. For example, <b><img border=0 width=18 height=13
     579src="manual_e.files/image019.jpg" alt=zoom1x.png></b>&nbsp;means 1 bp is
     580displayed by 1 pixel, whereas <b><img border=0 width=18 height=13
     581src="manual_e.files/image023.jpg" alt=zoom01x.png></b>&nbsp;means 10 bp is
     582displayed by 1 pixel. So <b><img border=0 width=18 height=13
     583src="manual_e.files/image018.jpg" alt=zoom10x.png></b>&nbsp;means the scale
     584that enlarges the display up to the base level.<span style='color:red'> </span><b><img
     585border=0 width=18 height=13 src="manual_e.files/image024.jpg"
     586alt=zoom0001x.png></b><span style='color:red'>&nbsp;</span>is a scale ratio
     587useful in displaying 1M bps on the screen.<span style='color:red'> </span>&nbsp;At
     588the time of scaling up or down the view points of the present display will be
     589remained unchanged.<span style='color:red'> </span></span></p>
     590
     591<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     592
     593<h3 style='text-align:justify;text-justify:inter-ideograph'><span lang=EN-US>Using
     594overview, ruler and zooming track method</span></h3>
     595
     596<p class=MsoNormal><span lang=EN-US>In addition, there are some methods to
     597shifting. These are overview, ruler, zooming trucks. You can shift the
     598viewpoint by clicking any position of these tracks. For details, please refer
     599to the respective details about the each track.</span></p>
     600
     601<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     602
     603<h2><span lang=EN-US>4.2. Functions of buttons</span></h2>
     604
     605<p class=MsoNormal style='margin-left:21.0pt;text-indent:-21.0pt'><span
     606lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     607</span></span><b><span lang=EN-US>(rev)&nbsp; </span></b><span lang=EN-US>You
     608can display the sequence in reverse mode by UT Genome Browser. Normally a sequence
     609is displayed from left to right but you can reverse it with the (rev) button. An
     610alternative way to display in reverse way is to input “start” value greater
     611than “end” value in the Input Box. The same task can be done easily by clicking
     612the (rev) button. As the (rev) button reverses start and end points of the
     613present displayed sequence so this can change the display mode from normal to
     614reverse or vice versa.<b> </b>If you press the (fasta) button on reverse mode,
     615then the complementary strand of displayed strand will be retrieved.</span></p>
     616
     617<p class=MsoNormal style='margin-left:21.0pt;text-indent:-21.0pt'><span
     618lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     619</span></span><b><span lang=EN-US>(top)&nbsp; </span></b><span lang=EN-US>By
     620pressing this button you can return to the main screen. Information about
     621present displayed range, track and each track setting etc. will be preserved.</span></p>
     622
     623<p class=MsoNormal style='margin-left:21.0pt;text-indent:-21.0pt'><span
     624lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     625</span></span><b><span lang=EN-US>(clear)&nbsp; </span></b><span lang=EN-US>By
     626pressing this button you can return to the main screen. Information about
     627present displayed range, track and each track setting etc. will be initialized.&nbsp;&nbsp;
     628</span></p>
     629
     630<p class=MsoNormal style='margin-left:21.0pt;text-indent:-21.0pt'><span
     631lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     632</span></span><b><span lang=EN-US>(Track)&nbsp; </span></b><span lang=EN-US>Addition,
     633deletion, and rearranging can be performed by this button. Details description
     634will be given later.</span></p>
     635
     636<p class=MsoNormal style='margin-left:21.0pt;text-indent:-21.0pt'><span
     637lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     638</span></span><b><span lang=EN-US>(fasta)&nbsp; </span></b><span lang=EN-US>Present
     639displaying sequence can be retrieved with this button in fasta format. You will
     640be instructed to save as a file name. For example,<b> </b>Medaka-200406-scaffold429
     641(64587-66612). fasta</span></p>
     642
     643<p class=MsoNormal><span lang=EN-US style='color:red'>&nbsp;</span></p>
     644
     645<h2><span lang=EN-US>4.3. Addition, Deletion, and Rearrangement of Tracks</span></h2>
     646
     647<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     648border=0 width=348 height=320 src="manual_e.files/image025.jpg"
     649alt="browser_track.png"></span></p>
     650
     651<p class=MsoNormal><b><span lang=EN-US style='font-size:14.0pt'>&nbsp;</span></b></p>
     652
     653<p class=MsoNormal><span lang=EN-US>When the (track) button of the main screen
     654is pressed, the above track-editing screen will pop up. Here you can do addition,
     655deletion and rearrangement of the tracks. This editing screen can be divided
     656into three parts - displaying tracks, removed tracks, and adding new track.</span></p>
     657
     658<p class=MsoNormal style='margin-left:31.5pt;text-indent:-21.0pt'><span
     659lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     660</span></span><b><span lang=EN-US>Displaying track: </span></b><span
     661lang=EN-US>Here, tracks’ deletion and rearrangement can be done to the present
     662displayed screen. The deleted tracks will be replaced to next removed track. </span></p>
     663
     664<p class=MsoNormal style='margin-left:31.5pt;text-indent:-21.0pt'><span
     665lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     666</span></span><b><span lang=EN-US>Removed track: </span></b><span lang=EN-US>This
     667is the list of all tracks, which are deleted at Displaying Tracks. It is something
     668like garbage bin. Undo-processing is possible for the tracks that are displayed
     669here.</span></p>
     670
     671<p class=MsoNormal style='margin-left:31.5pt;text-indent:-21.0pt'><span
     672lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     673</span></span><b><span lang=EN-US>Add new track: </span></b><span lang=EN-US>New
     674tracks, which are not available at present display, can be added by this track.
     675By setting the URL of the new tracks, push add button. If the new tracks’ URL
     676is read properly, the new tracks will be added after the present displayed
     677tracks.&nbsp; </span></p>
     678
     679<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     680
     681<h2><span lang=EN-US>4.4. Setting for Tracks</span></h2>
     682
     683<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     684border=0 width=358 height=288 src="manual_e.files/image026.jpg"></span></p>
     685
     686<p class=MsoNormal><span lang=EN-US>On main screen, when the <img border=0
     687width=9 height=9 src="manual_e.files/image027.jpg" alt=cfg.png>&nbsp;button,
     688beside the track name, is pressed, the display of that track can be customized
     689as above image. The customizing contents of the tracks differ from each other.
     690On the other hand, there are some tracks which contents cannot be customized at
     691all. For details, please refer to the individual tracks information.&nbsp;&nbsp;
     692</span></p>
     693
     694<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     695
     696<h1><span lang=EN-US>5. Pre-defined Tracks</span></h1>
     697
     698<h2><span lang=EN-US>5.1. Overview Track</span></h2>
     699
     700<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     701border=0 width=552 height=15 src="manual_e.files/image028.jpg"
     702alt="track_overview.png"></span></p>
     703
     704<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US
     705style='font-size:12.0pt;font-family:"MS 明朝"'>&nbsp;</span></p>
     706
     707<p class=MsoNormal><span lang=EN-US>This track shows the range of present
     708displayed window in the total genome. In above image, for instance, the
     709blue-colored viewpoint shows the range from 125kb to 145kb. Clicking on any
     710position of this overview track moves the viewpoint the middle position. For
     711example, when you click on around 100k positions, the viewpoint will move to
     71290k-110k. </span></p>
     713
     714<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     715
     716<h2><span lang=EN-US>5.2. Ruler and Zooming Tracks</span></h2>
     717
     718<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     719border=0 width=566 height=9 src="manual_e.files/image029.jpg"></span></p>
     720
     721<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     722border=0 width=566 height=9 src="manual_e.files/image030.jpg"></span></p>
     723
     724<p class=MsoNormal><span lang=EN-US>Both the ruler track and the zooming track
     725are displaying same contents with different color. These two show the base
     726position number of the present displayed content with respect to the total
     727sequence.&nbsp; If you click any position of the ruler track, the viewpoint
     728will move to the middle position. For example, if the rightmost end of the
     729ruler track is clicked then the same effect will be happed as the <img
     730border=0 width=15 height=10 src="manual_e.files/image031.jpg" alt=ff.png>&nbsp;button
     731of main screen is pressed. Before using the zoom button on main screen, it is
     732better to have the required region on middle position by using the ruler track
     733to smoothing future enlarge processing.</span></p>
     734
     735<p class=MsoNormal style='text-indent:5.25pt'><span lang=EN-US>In addition to
     736the effect of the ruler track, if you click any position on the zooming track
     737then two times zoom will be happened. For example, it is same to click the
     738central button on zoom track as the <img border=0 width=13 height=13
     739src="manual_e.files/image017.jpg" alt=zoomin.png>&nbsp;button on main screen.
     740On the other hand, it is also same to clicking the rightmost end of the zooming
     741track as click <img border=0 width=18 height=13
     742src="manual_e.files/image014.jpg" alt=ff.png>&nbsp;then click <img border=0
     743width=13 height=13 src="manual_e.files/image017.jpg" alt=zoomin.png>&nbsp;on
     744main screen. This track is useful to zoom out our interested region on the
     745sequence..</span></p>
     746
     747<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     748
     749<h2><span lang=EN-US>5.3. Base Color Track</span></h2>
     750
     751<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     752border=0 width=566 height=9 src="manual_e.files/image032.jpg"><img border=0
     753width=566 height=9 src="manual_e.files/image033.jpg"></span></p>
     754
     755<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US>&nbsp;</span></p>
     756
     757<p class=MsoNormal><span lang=EN-US>Base color track changes the sequence to
     758color mode. All four ATGC bases are displayed by converting to the individual color.
     759It is natural to display each base pair by one pixel. By zooming in, you can
     760see any specific region of the sequence in alphabet symbol (above bottom
     761image). </span></p>
     762
     763<p class=MsoNormal style='text-indent:5.25pt'><span lang=EN-US>It is also possible
     764to customize the corresponding base pair color also. For example, if GC base
     765pair are only colored then we can use it as a simple GC content track. To get
     766the sequence itself, it is better to save from fasta track.</span></p>
     767
     768<p class=MsoNormal><span lang=EN-US style='color:red'>&nbsp;</span></p>
     769
     770<h2><span lang=EN-US>5.4. Gap Track</span></h2>
     771
     772<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     773border=0 width=566 height=7 src="manual_e.files/image034.jpg"></span></p>
     774
     775<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US>&nbsp;</span></p>
     776
     777<p class=MsoNormal><span lang=EN-US>Gap Track is a track that displays gaps in
     778a scaffold. By clicking any place except the gap, we can get the whole contig
     779sequence in FASTA format. It is different from the (fasta) button in the main
     780window, because it does not retrieve the displayed sequence only, but saves the
     781whole contig sequence.</span></p>
     782
     783<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     784
     785<h2><span lang=EN-US>5.5. GC Content Track</span></h2>
     786
     787<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     788border=0 width=566 height=28 src="manual_e.files/image035.jpg"></span></p>
     789
     790<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     791
     792<p class=MsoNormal><span lang=EN-US>This track displays the ratio of GC
     793contents for 5 pixels. If the pixel number of a base pair is more than 5, the
     794coloring will be done to tell whether it is GC or AT. </span></p>
     795
     796<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     797
     798<h2><span lang=EN-US>5.6. Mapped Gene Track</span></h2>
     799
     800<p class=MsoNormal align=center style='margin-right:-60.8pt;text-align:center'><span
     801lang=EN-US><img border=0 width=566 height=58 src="manual_e.files/image036.jpg"></span></p>
     802
     803<p class=MsoNormal style='margin-right:-60.8pt'><span lang=EN-US>&nbsp;</span></p>
     804
     805<p class=MsoNormal><span lang=EN-US>This track displays the mapping result of
     806Fugu, Zebra fish and Medaka’s Est to the Medaka genome, done by ALPS (<a href="http://alps.gi.k.u-tokyo.ac.jp">http://alps.gi.k.u-tokyo.ac.jp</a>). The
     807mapping region for the gene is displayed by line and the exons are shown in rectangular
     808box. The arrow sign shows the plus or minus strand of the genome. The above
     809image displays Medaka’s ESTs in black color, while the green color indicates
     810cDNAs of Fugu. The current data sources of mapped genes are Medaka Unigene
     811Build#10, Zebra fish Unigene Build#71, and Fugu ensemble pufferfish v21.2.c1(
     81210<sup>th</sup> May, 2004). We will revise the alignment periodically in
     813response to the update of the data sources.</span></p>
     814
     815<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     816
     817<h3 style='text-align:justify;text-justify:inter-ideograph'><span lang=EN-US>Display
     818setting</span></h3>
     819
     820<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     821border=0 width=358 height=288 src="manual_e.files/image037.jpg"></span></p>
     822
     823<p class=MsoNormal><span lang=EN-US>If the <img border=0 width=9 height=9
     824src="manual_e.files/image027.jpg" alt=cfg.png>&nbsp;button on the left side of
     825Mapped Gene Track is pressed, the display setting windows will pop up. There
     826are three parts of this setting; namely, changing the total display style,
     827alternating the mapping results if a gene will be displayed or not, and modifying
     828the color of a gene. The setting, whether to show or not, will display all
     829which fulfill the conditions. The color setting can be done by “use this color”
     830button beside the track.&nbsp; </span></p>
     831
     832<p class=MsoNormal><b><span lang=EN-US>Style select setting</span></b></p>
     833
     834<p class=MsoNormal><span lang=EN-US>Predicted genes’ display setting can be
     835changed here. There are four kinds of display style. These styles are full,
     836pack, small and dense. </span></p>
     837
     838<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     839lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     840</span></span><b><span lang=EN-US>Full:</span></b><span lang=EN-US> In full
     841style, each gene’s position is displayed on one line. On left side the Genebank
     842accession number or Ensemble Gene ID is written. <br>
     843<img border=0 width=489 height=156 src="manual_e.files/image038.jpg"></span></p>
     844
     845<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     846lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     847</span></span><b><span lang=EN-US>Pack:</span></b><span lang=EN-US> By showing
     848individual alignments together with the names (Genebank Acc or Ensemble Gene
     849ID) of genes on left side in multiple on one line, the pack style is more
     850compact than full style.<br>
     851<img border=0 width=488 height=50 src="manual_e.files/image039.jpg"></span></p>
     852
     853<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     854lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     855</span></span><b><span lang=EN-US>Small:</span></b><span lang=EN-US> In small
     856style, the up and down spaces for one gene are reduced to the minimum. Unlike
     857the full style and the pack style, this does not display the names of the
     858genes.<br>
     859
     860<img border=0 width=488 height=17 src="manual_e.files/image040.jpg"></span></p>
     861
     862<p class=MsoNormal style='margin-left:42.0pt;text-indent:-21.0pt'><span
     863lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     864</span></span><b><span lang=EN-US>Dense:</span></b><span lang=EN-US> In this
     865style, only the positions of aligned exons are displayed on one line.<br>
     866<img border=0 width=484 height=8 src="manual_e.files/image041.jpg"></span></p>
     867
     868<p class=MsoNormal><span lang=EN-US>At present except the full style, if the
     869numbers of the mapped genes are more than 200 in a range of more than 50kbp, the
     870graphical view of the genes will be displayed.</span></p>
     871
     872<p class=MsoNormal><b><span lang=EN-US>FormSpecies disp setting</span></b></p>
     873
     874<p class=MsoNormal><span lang=EN-US>Here we can set which species among Medaka,
     875Zebra fish, Fugu’s mapping results are displayed or not. On default, all
     876species results will be displayed. Only the species, which are checked on the
     877Checkbook, will be displayed.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></p>
     878
     879<p class=MsoNormal><b><span lang=EN-US>FromSpecies color setting </span></b></p>
     880
     881<p class=MsoNormal><span lang=EN-US>The color distinguishing for Medaka, Zebra
     882fish, Fugu’s can be done here.</span></p>
     883
     884<p class=MsoNormal><b><span lang=EN-US>MatchRatio gradation setting</span></b></p>
     885
     886<p class=MsoNormal><span lang=EN-US>Gene’s color can be changed with respect to
     887its match ratio. Provided colors for the match ratios 0.7 and 1.0 respectively,
     888the system automatically gradates the coloring of the alignments between the
     889lower and upper match ratios.&nbsp;&nbsp; </span></p>
     890
     891<p class=MsoNormal><b><span lang=EN-US>MatchRatio ulbound setting</span></b></p>
     892
     893<p class=MsoNormal><span lang=EN-US>You can specify the range of the mapping
     894ratio by inputting the lower and upper bounds into the corresponding boxes.
     895Alignments of match ratios within the range are only displayed.</span></p>
     896
     897<p class=MsoNormal><b><span lang=EN-US>CoverRatio gradation setting</span></b></p>
     898
     899<p class=MsoNormal><span lang=EN-US>Gene’s color can also be changed with
     900respect to its cover ratio. Provided colors for the cover ratios 0.4 and 1.0
     901respectively, the system automatically gradates the coloring of the alignments
     902between the lower and upper cover ratios.&nbsp;&nbsp; </span></p>
     903
     904<p class=MsoNormal><b><span lang=EN-US>CoverRatio ulbound setting</span></b></p>
     905
     906<p class=MsoNormal><span lang=EN-US>You can specify the range of the cover
     907ratio by inputting the lower and upper bounds into the corresponding boxes.
     908Alignments of cover ratios within the range are only displayed.</span></p>
     909
     910<p class=MsoNormal><b><span lang=EN-US>Stage disp setting</span></b></p>
     911
     912<p class=MsoNormal><span lang=EN-US>Here, you can fix which development stage’s
     913expression EST should be displayed.&nbsp; </span></p>
     914
     915<p class=MsoNormal><b><span lang=EN-US>Stage color setting</span></b></p>
     916
     917<p class=MsoNormal><span lang=EN-US>Color distinguishing can be done with
     918respect to development stage.</span></p>
     919
     920<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     921
     922<h3 style='text-align:justify;text-justify:inter-ideograph'><span lang=EN-US>Linkage
     923for each gene </span></h3>
     924
     925<p class=MsoNormal><span lang=EN-US>In full, pack and small style, each gene
     926can be clicked on. By clicking each gene, you can see the details of this gene.</span></p>
     927
     928<p class=MsoNormal><b><span lang=EN-US style='font-size:14.0pt'>&nbsp;</span></b></p>
     929
     930<h2><span lang=EN-US>5.7. Genscan Track</span></h2>
     931
     932<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     933border=0 width=567 height=39 src="manual_e.files/image042.jpg"></span></p>
     934
     935<p class=MsoNormal><span lang=EN-US>This track displays the predicted genes by
     936Genscan. The predicted genes are viewed on lines, where the exons parts are on rectangular
     937shape. Arrow sign presents the strand of the genes. The above image shows the
     938predicted genes in pack style. </span></p>
     939
     940<p class=MsoNormal><b><span lang=EN-US>Display settings</span></b></p>
     941
     942<p class=MsoNormal><span lang=EN-US>If the <img border=0 width=9 height=9
     943src="manual_e.files/image027.jpg" alt=cfg.png>&nbsp;mark button on the left
     944side of Genscan Track is clicked, the display setting will pop up. Here are the
     945details of this setting. </span></p>
     946
     947<p class=MsoNormal><b><span lang=EN-US>Style selects setting</span></b></p>
     948
     949<p class=MsoNormal><span lang=EN-US>Predicted genes’ display setting can be
     950changed here. There are four kinds of display style. These styles are full,
     951pack, small and dense, and they are similar to those styles in Mapped Gene
     952Track.</span></p>
     953
     954<p class=MsoNormal><b><span lang=EN-US>Linkage of each gene</span></b></p>
     955
     956<p class=MsoNormal><span lang=EN-US>In full, pack and small style each gene can
     957be clicked on. After clicking each gene, the details of prediction by Genscan
     958will be appeared.</span></p>
     959
     960<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     961
     962<h2><span lang=EN-US>5.8. Comparative Genomics Track</span></h2>
     963
     964<p class=MsoNormal><b><span lang=EN-US style='font-size:12.0pt'>Fugu Scaffold
     965track</span></b></p>
     966
     967<p class=MsoNormal><b><span lang=EN-US>Description</span></b></p>
     968
     969<p class=MsoNormal><span lang=EN-US>This track shows Fugu/Medaka homologous
     970scaffolds detected by ALPS alignment program. Fugu scaffolds are denoted by
     971boxes connected by arrows. The boxes represent regions of high homology (match
     972ratio &gt; 60%) aligned by ALPS. The arrows represent low homology regions or
     973gaps in Fugu scaffold.&nbsp; The direction of arrows indicates the orientation
     974of Fugu/Medaka alignments. Clicking on a Fugu scaffold will open a new window
     975to display its dotplot with Fugu scaffold sequence provided in the same page.&nbsp;
     976The Fugu sequence (Fugu v.2.0) was downloaded from JGI.</span></p>
     977
     978<p class=MsoNormal><b><span lang=EN-US>Method</span></b></p>
     979
     980<p class=MsoNormal><span lang=EN-US>Fugu scaffold sequences are split into
     981non-overlapping 300mer sequences and these 300mer sequences are mapped to
     982Medaka scaffolds with ALPS. ALPS alignments with match ratio less than 60% are
     983discarded and remaining alignments are chained by longest monotone subsequence
     984algorithm. Chains consist of more than 10 alignments are displayed in the
     985track. Note that inversions or microrearrangements are not shown. Only the longest
     986monotone subsequence is displayed for each Fugu scaffold.</span></p>
     987
     988<p class=MsoNormal><b><span lang=EN-US>Linkage of each scaffold </span></b></p>
     989
     990<p class=MsoNormal><span lang=EN-US>In full, pack and small style each gene can
     991be clicked on. After clicking each scaffold, the detailed alignments will be
     992appeared as like dot plot. Dotplot shows homologous regions of Fugu/Medaka
     993scaffolds as diagonal runs of dots. Each dot, plotted based on sequence
     994similarity score, indicates that significantly many seed matches are found
     995between corresponding regions. The sequence similarity score is defined in such
     996a way that tandem repeats are not assigned high scores while unique sequences
     997are assigned high scores.</span></p>
     998
     999<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US><img
     1000border=0 width=567 height=201 src="manual_e.files/image043.jpg"></span></p>
     1001
     1002<p class=MsoNormal align=center style='text-align:center'><span lang=EN-US>&nbsp;</span></p>
     1003
     1004<p class=MsoNormal align=center style='text-align:center'><b><span lang=EN-US>&nbsp;</span></b></p>
     1005
     1006<span lang=EN-US style='font-size:10.5pt;font-family:Century'><br clear=all
     1007style='page-break-before:always'>
     1008
     1009</span>
     1010
     1011<p class=MsoNormal><b><span lang=EN-US style='font-size:14.0pt'>Ramen Assembler
     1012/ UT Genome Browser Team Members</span></b></p>
     1013
     1014<p class=MsoNormal><span lang=EN-US><br>
     1015Ramen Genome Assembler Development Team</span></p>
     1016
     1017<p class=MsoNormal style='margin-left:21.0pt;text-indent:-21.0pt'><span
     1018lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     1019</span></span><span lang=EN-US>Development of “Ramen” genome assembler and
     1020assembly of medaka genome:<br>
     1021Masahiro Kasahara and Shin Sasaki</span></p>
     1022
     1023<p class=MsoNormal style='margin-left:21.0pt;text-indent:-21.0pt'><span
     1024lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     1025</span></span><span lang=EN-US>Development of “Ramen Viewer” for genome
     1026assembly: <br>
     1027
     1028Yukinobu Nagayasu</span></p>
     1029
     1030<p class=MsoNormal><span lang=EN-US><br>
     1031UT Genome Browser Development Team</span></p>
     1032
     1033<p class=MsoNormal style='margin-left:21.0pt;text-indent:-21.0pt'><span
     1034lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     1035</span></span><span lang=EN-US>Design and development of UT Genome Browser,
     1036keyword search function, libraries for describing tracks: <br>
     1037Yukinobu Nagayasu and Koichiro Doi</span></p>
     1038
     1039<p class=MsoNormal style='margin-left:21.0pt;text-indent:-21.0pt'><span
     1040lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     1041</span></span><span lang=EN-US>Online mapping function for query sequences:<br>
     1042Tomoyuki Yamada</span></p>
     1043
     1044<p class=MsoNormal style='margin-left:21.0pt;text-indent:-21.0pt'><span
     1045lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     1046</span></span><span lang=EN-US>Comparative Genomics Track:<br>
     1047Yoichiro Nakatani and Wei Qu</span></p>
     1048
     1049<p class=MsoNormal style='margin-left:21.0pt;text-indent:-21.0pt'><span
     1050lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     1051</span></span><span lang=EN-US>Gene Prediction:<br>
     1052Ahsan Budrul</span></p>
     1053
     1054<p class=MsoNormal style='margin-left:21.0pt;text-indent:-21.0pt'><span
     1055lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     1056</span></span><span lang=EN-US>Mapped Gene Track:<br>
     1057Yasuhiro Kasai</span></p>
     1058
     1059<p class=MsoNormal style='margin-left:21.0pt;text-indent:-21.0pt'><span
     1060lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     1061</span></span><span lang=EN-US>Database access accelerators:<br>
     1062Takehiro Furudate and Atsushi Mori</span></p>
     1063
     1064<p class=MsoNormal style='margin-left:21.0pt;text-indent:-21.0pt'><span
     1065lang=EN-US style='font-family:Wingdings'>&uuml;<span style='font:7.0pt "Times New Roman"'>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
     1066</span></span><span lang=EN-US>Overall management:<br>
     1067Koichiro Doi and Shinichi Morishita</span></p>
     1068
     1069<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>
     1070
     1071<p class=MsoNormal><b><span lang=EN-US style='font-size:14.0pt'>Acknowledgements</span></b></p>
     1072
     1073<p class=MsoNormal><b><span lang=EN-US style='font-size:14.0pt'>&nbsp;</span></b></p>
     1074
     1075<p class=MsoNormal><span lang=EN-US>This work has been supported by
     1076Grant-in-Aid for Scientific Research on Priority Areas (Grant#12209003) to
     1077Shinichi Morishita. </span></p>
     1078
     1079<p class=MsoNormal><span lang=EN-US>Ramen Assembler Development Team members
     1080are indebted to Yuji Kohara and Tadasu Shin-i for their technical discussions
     1081on the whole genome shotgun assembly.</span></p>
     1082
     1083<p class=MsoNormal><span lang=EN-US>Members in the UT Genome Browser
     1084Development Team are grateful to Kiyoshi Naruse, Daisuke Kobayashi, and
     1085Takanori Narita for their valuable input to improve the functions of the
     1086browser in a variety of ways.</span></p>
     1087
     1088</div>
     1089}}}