Difference between revisions of "Preparing and loading data"

Latest revision as of 17:21, 9 January 2014

There are several easy ways to load up data into GenomeView. Before you load your data, you may want to make sure you're using a supported format from the list below. Generally, GenomeView will notify you if it doesn't understand your data.

Loading data

You can load your data files ...

... by selecting "work with my data" in the Genome Explorer
... by dragging them onto GenomeView
... by selecting the 'File' menu and then 'Load data...' (tutorial)
... by pressing CTRL+O
... by specifying them as argument on the command-line
... by loading a session file

You can load preloaded data ...

... by selecting a genome from the Genome Explorer
... following a link from a GenomeView enabled website

Data preparation recipe

Match identifiers: GenomeView uses the identifiers to link different sources, so make sure that the identifiers match (case-sensitive).
Create indices for data files that need it (check table below)
Convert file formats to get desired visuals (check table below)
Load data (see above)

Why index files? Indexing will create a look-up table for GenomeView to load data on-the-fly. This will will speed up browsing and loading speed, as well as significantly reduce the amount of memory you need. For some file formats we recommend you create indices, for other we do not. See the table below for more details and links to instructions.

Recommended file formats

This is a list of file formats that are recommended for different data types. See the full list of data types in the section below.

Data type	Recommended file format	Instructions
Reference sequence	fasta	Preparing reference sequence
Annotation	GFF3	Preparing annotation
Read a alignments	BAM	Preparing read data
Variation	VCF	Preparing VCF data
Coverage summary - continuous values	TDF	Preparing value data
Whole genome alignments	MAF	Preparing whole genome alignments
Genome synteny	experimental	Preparing genome synteny

Supported data formats

Reference sequence

Data type	File format	Index*	Max size**		Comments
			unindexed***	indexed
Reference sequence	fasta ^¤	Recommended Index FASTA	50 Mb	unlimited	GenomeView will query the user create index for you if you don't have one and the file is very large.
Reference sequence	embl, genbank	Not possible	50 Mb	--	EMBL and genbank are mixed file formats that can contain both annotation and reference sequence at the same time.

Annotation

Data type	File format	Index*	Max size**		Comments
Annotation	gff ^¤	Not recommended Index GFF	50 Mb	unlimited
	embl, genbank	Not possible	50 Mb	--	EMBL and genbank are mixed file formats that can contain both annotation and reference sequence at the same time.
	bed	Not recommended Index BED	50 Mb or less	unlimited	By default data from a bed file is added to the CDS track, if you want it in a different track, you have to add a line a the top of the file 'track name=Track_name'. No white-space is allowed in the track name.
	ptt, tbl	Not possible	50 Mb or less	--	Other standard annotation formats GenomeView understands
	various formats	Not possible	50 Mb or less	--	GenomeView can directly parse the output of the following programs: Blast, GeneMark, TransTermHP, FindPeaks, MaqSNP, tRNA-scan

Whole genome alignments

Data type	File format	Index*	Max size**		Comments
Multiple genome alignment	maf ^¤	Recommended	100 Mb	unlimited	GenomeView will prompt you to create a compressed maf file and index it for you, if you're trying to load an unindexed maf file. MAF is the recommended file format for whole genome alignemnt of large/complex genomes
	multi-fasta ^¤	Not possible	100 Mb	--	Recommended for small/simple genomes with a near 1:1 relationship.
	aln, ClustalW	Not possible	100 Mb	--

Read alignments

Data type	File format	Index*	Max size**		Comments
Sequence read alignment	bam ^¤ Preparing read data	Required	--	unlimited	GenomeView will prompt you if there is no index and will create one for you. GenomeView can not automatically sort BAM files.
Sequence read alignment	MAQ, MapView, BroadSolexa	Not possible	100 Mb	--

Read coverage summary - continuous value data

Data type	File format	Index*	Max size**		Comments
Read coverage summary	tdf ^¤	Native	unlimited	unlimited	TDF files can be created with the bam2tdf tool that is available for download.
	bigwig	Native	unlimited	unlimited	This format can be used for any wig file, not just read coverage
	pileup	Required	--	unlimited	The pileup format becomes slow when you have extreme read depth (>5000 x coverage)
	wig	Not possible	50 Mb	--	We strongly recommend to convert your wig files to TDF. GenomeView can automatically convert wig files to TDF. Caveats: 'track' information should all be on a single line, 'browser' lines will be ignored as the are specific to the UCSC Genome Browser. WIG files need to be sorted by chromosome and by genomic coordinate within the chromosome. BedGraph as well as Wiggle_0 format is supported. For the wiggle_0 type, both variableStep and fixedStep should work.

Genome variation and diversity

Data type	File format	Index*	Max size**		Comments
Genome variation	vcf ^¤	Not recommended	--	unlimited	It is recommended to run reducevcf on VCF prior to loading them, this will speed up the loading time significantly.

Allele diversity

Data type	File format	Index*	Max size**		Comments
Allele diversity summary	pileup ^¤	Required	--	unlimited	The pileup format becomes slow when you have extreme read depth (>5000 x coverage)

* Indicates whether this file format can/should be indexed. 

** Recommended maximum file size. First value is without index, the second with index. This values are only guidelines. When loading multiple data sets, you should add the sizes.

*** Unindexed data files can be gzip compressed.

^¤ Recommended file format for this data type.

Output formats

(Modified) annotations can be saved as either GFF or EMBL.

All data that is loaded can be exported in their original format. This will not include modifications.

Converting formats

<a href="http://genomeview.org/loki/">We offer a few tools to convert files between formats.</a>

Previous documentation pages

Supported data formats Fasta files

Feature files

Read data

Coverage plots

@@ Line 3: / Line 3: @@
-==Recipe==
+There are several easy ways to load up data into GenomeView. Before you load your data, you may want to make sure you're using a supported format from the list below. Generally, GenomeView will notify you if it doesn't understand your data.
+==Loading data ==
+You can load your data files ...
+* ... by selecting "work with my data" in the [[Genome Explorer]]
+* ... by dragging them onto GenomeView
+* ... by selecting the 'File' menu and then 'Load data...' ([http://genomeview.org/content/load-data tutorial])
+* ... by pressing CTRL+O
+* ... by specifying them as argument on the [[command-line use|command-line]]
+* ... by loading a [[session file]]
+You can load preloaded data ...
+* ... by selecting a genome from the [[Genome Explorer]]
+* ... following a link from a [[Integration|GenomeView enabled website]]
+==Data preparation recipe==
 # Match identifiers: GenomeView uses the identifiers to link different sources, so make sure that the identifiers match (case-sensitive).
 # Create indices for data files that need it (check table below)
 # Convert file formats to get desired visuals (check table below)
-# Load data
+# Load data (see above)
+'''Why index files?''' Indexing will create a look-up table for GenomeView to load data on-the-fly. This will will speed up browsing and loading speed, as well as significantly reduce the amount of memory you need. For some file formats we recommend you create indices, for other we do not. See the table below for more details and links to instructions.
+==Recommended file formats ==
+This is a list of file formats that are recommended for different data types. See the full list of data types in the section below.
-== Why index files? ==
-Indexing will create a look-up table for GenomeView to load data on-the-fly. This will will speed up browsing and loading speed, as well as significantly reduce the amount of memory you need. For some file formats we recommend you create indices, for other we do not. See the table below for more details and links to instructions.
+<table border=1>
+<tr><th>Data type</th><th>Recommended file format</th><th>Instructions</th></tr>
+<tr><td>Reference sequence</td><td>fasta</td><td>[[Preparing reference sequence]]</td></tr>
+<tr><td>Annotation</td><td>GFF3</td><td>[[Preparing annotation]]</td></tr>
+<tr><td>Read a alignments</td><td>BAM</td><td>[[Preparing read data]]</td></tr>
+<tr><td>Variation</td><td>VCF</td><td>[[Preparing VCF data]]</td></tr>
+<tr><td>Coverage summary - continuous values</td><td>TDF</td><td>[[Preparing value data]]</td></tr>
+<tr><td>Whole genome alignments</td><td>MAF</td><td>[[Preparing whole genome alignments]]</td></tr>
+<tr><td>Genome synteny</td><td>experimental</td><td>[[Preparing genome synteny]]</td></tr>
+</table>
 == Supported data formats ==
@@ Line 54: / Line 86: @@
 <table border=1>
 <tr><th>Data type</th><th>File format</th><th>Index*</th><th colspan=2>Max size**</th><th>Comments</th></tr>
-<tr><td valign="top" rowspan=2>Sequence read alignment</td><td><b><a href="/content/preparing-short-read-alignments">bam</a></b> <sup>&#164;</sup></td><td>Required</td><td>--</td><td>unlimited</td><td>GenomeView will prompt you if there is no index and will create one for you.</td></tr>
+<tr><td valign="top" rowspan=2>Sequence read alignment</td><td><b>bam</b> <sup>&#164;</sup><br>[[Preparing read data]]</td><td>Required</td><td>--</td><td>unlimited</td><td>GenomeView will prompt you if there is no index and will create one for you. GenomeView can not automatically sort BAM files.</td></tr>
 <tr><td>MAQ, MapView, BroadSolexa</td><td>Not possible</td><td>100 Mb</td><td>--</td></tr>
 </table>
-=== Read coverage summary ===
+=== Read coverage summary - continuous value data ===
 <table border=1>
 <tr><th>Data type</th><th>File format</th><th>Index*</th><th colspan=2>Max size**</th><th>Comments</th></tr>
@@ Line 71: / Line 103: @@
 GenomeView can automatically convert wig files to TDF. Caveats: 'track' information should all be on a single line, 'browser' lines will be ignored as the are specific to the UCSC Genome Browser. WIG files need to be sorted by chromosome and by genomic coordinate within the chromosome. BedGraph as well as Wiggle_0 format is supported. For the wiggle_0 type, both variableStep and fixedStep should work.</td></tr>
 </table>
+=== Genome variation and diversity ===
+<table border=1>
+<tr><th>Data type</th><th>File format</th><th>Index*</th><th colspan=2>Max size**</th><th>Comments</th></tr>
+<tr><td>Genome variation</td><td><b> [[vcf]]</b> <sup>&#164;</sup></td><td>Not recommended</td><td>--</td><td>unlimited</td><td>It is recommended to run [[reducevcf]] on VCF prior to loading them, this will speed up the loading time significantly.</td></tr>
+</table>
 === Allele diversity ===
 <table border=1>
 <tr><th>Data type</th><th>File format</th><th>Index*</th><th colspan=2>Max size**</th><th>Comments</th></tr>
-<tr><td>Allele diversity summary</td><td><b> <a href="/content/preparing-pileup#pileup">pileup</a></b> <sup>&#164;</sup></td><td>Required</td><td>--</td><td>unlimited</td><td>The pileup format becomes slow when you have extreme read depth (>5000 x coverage)</td></tr>
+<tr><td>Allele diversity summary</td><td><b> [[pileup]]</b> <sup>&#164;</sup></td><td>Required</td><td>--</td><td>unlimited</td><td>The pileup format becomes slow when you have extreme read depth (>5000 x coverage)</td></tr>
 </table>
@@ Line 97: / Line 137: @@
 == Previous documentation pages ==
-[http://genomeview.org/content/load-data Load data tutorial]
 [http://genomeview.org/content/data-formats Supported data formats]