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tabix(1) [debian man page]

tabix(1)						       Bioinformatics tools							  tabix(1)

NAME
bgzip - Block compression/decompression utility tabix - Generic indexer for TAB-delimited genome position files SYNOPSIS
bgzip [-cdhB] [-b virtualOffset] [-s size] [file] tabix [-0lf] [-p gff|bed|sam|vcf] [-s seqCol] [-b begCol] [-e endCol] [-S lineSkip] [-c metaChar] in.tab.bgz [region1 [region2 [...]]] DESCRIPTION
Tabix indexes a TAB-delimited genome position file in.tab.bgz and creates an index file in.tab.bgz.tbi when region is absent from the com- mand-line. The input data file must be position sorted and compressed by bgzip which has a gzip(1) like interface. After indexing, tabix is able to quickly retrieve data lines overlapping regions specified in the format "chr:beginPos-endPos". Fast data retrieval also works over network if URI is given as a file name and in this case the index file will be downloaded if it is not present locally. OPTIONS OF TABIX
-p STR Input format for indexing. Valid values are: gff, bed, sam, vcf and psltab. This option should not be applied together with any of -s, -b, -e, -c and -0; it is not used for data retrieval because this setting is stored in the index file. [gff] -s INT Column of sequence name. Option -s, -b, -e, -S, -c and -0 are all stored in the index file and thus not used in data retrieval. [1] -b INT Column of start chromosomal position. [4] -e INT Column of end chromosomal position. The end column can be the same as the start column. [5] -S INT Skip first INT lines in the data file. [0] -c CHAR Skip lines started with character CHAR. [#] -0 Specify that the position in the data file is 0-based (e.g. UCSC files) rather than 1-based. -h Print the header/meta lines. -B The second argument is a BED file. When this option is in use, the input file may not be sorted or indexed. The entire input will be read sequentially. Nonetheless, with this option, the format of the input must be specificed correctly on the command line. -f Force to overwrite the index file if it is present. -l List the sequence names stored in the index file. EXAMPLE
(grep ^"#" in.gff; grep -v ^"#" in.gff | sort -k1,1 -k4,4n) | bgzip > sorted.gff.gz; tabix -p gff sorted.gff.gz; tabix sorted.gff.gz chr1:10,000,000-20,000,000; NOTES
It is straightforward to achieve overlap queries using the standard B-tree index (with or without binning) implemented in all SQL data- bases, or the R-tree index in PostgreSQL and Oracle. But there are still many reasons to use tabix. Firstly, tabix directly works with a lot of widely used TAB-delimited formats such as GFF/GTF and BED. We do not need to design database schema or specialized binary formats. Data do not need to be duplicated in different formats, either. Secondly, tabix works on compressed data files while most SQL databases do not. The GenCode annotation GTF can be compressed down to 4%. Thirdly, tabix is fast. The same indexing algorithm is known to work effi- ciently for an alignment with a few billion short reads. SQL databases probably cannot easily handle data at this scale. Last but not the least, tabix supports remote data retrieval. One can put the data file and the index at an FTP or HTTP server, and other users or even web services will be able to get a slice without downloading the entire file. AUTHOR
Tabix was written by Heng Li. The BGZF library was originally implemented by Bob Handsaker and modified by Heng Li for remote file access and in-memory caching. SEE ALSO
samtools(1) tabix-0.2.0 11 May 2010 tabix(1)

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BP_PROCESS_GADFLY(1p)					User Contributed Perl Documentation				     BP_PROCESS_GADFLY(1p)

NAME
process_gadfly.pl - Massage Gadfly/FlyBase GFF files into a version suitable for the Generic Genome Browser SYNOPSIS
% process_gadfly.pl ./RELEASE2 > gadfly.gff DESCRIPTION
This script massages the RELEASE 3 Flybase/Gadfly GFF files located at http://www.fruitfly.org/sequence/release3download.shtml into the "correct" version of the GFF format. To use this script, download the whole genome FASTA file and save it to disk. (The downloaded file will be called something like "na_whole-genome_genomic_dmel_RELEASE3.FASTA", but the link on the HTML page doesn't give the filename.) Do the same for the whole genome GFF annotation file (the saved file will be called something like "whole-genome_annotation-feature-region_dmel_RELEASE3.GFF".) If you wish you can download the ZIP compressed versions of these files. Next run this script on the two files, indicating the name of the downloaded FASTA file first, followed by the gff file: % process_gadfly.pl na_whole-genome_genomic_dmel_RELEASE3.FASTA whole-genome_annotation-feature-region_dmel_RELEASE3.GFF > fly.gff The gadfly.gff file and the fasta file can now be loaded into a Bio::DB::GFF database using the following command: % bulk_load_gff.pl -d fly -fasta na_whole-genome_genomic_dmel_RELEASE3.FASTA fly.gff (Where "fly" is the name of the database. Change it as appropriate. The database must already exist and be writable by you!) The resulting database will have the following feature types (represented as "method:source"): Component:arm A chromosome arm Component:scaffold A chromosome scaffold (accession #) Component:gap A gap in the assembly clone:clonelocator A BAC clone gene:gadfly A gene accession number transcript:gadfly A transcript accession number translation:gadfly A translation codon:gadfly Significance unknown exon:gadfly An exon symbol:gadfly A classical gene symbol similarity:blastn A BLASTN hit similarity:blastx A BLASTX hit similarity:sim4 EST->genome using SIM4 similarity:groupest EST->genome using GROUPEST similarity:repeatmasker A repeat IMPORTANT NOTE: This script will *only* work with the RELEASE3 gadfly files and will not work with earlier releases. SEE ALSO
Bio::DB::GFF, bulk_load_gff.pl, load_gff.pl AUTHOR
Lincoln Stein, lstein@cshl.org Copyright (c) 2002 Cold Spring Harbor Laboratory This library is free software; you can redistribute it and/or modify it under the same terms as Perl itself. See DISCLAIMER.txt for disclaimers of warranty. perl v5.14.2 2012-03-02 BP_PROCESS_GADFLY(1p)
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