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tabix(1) |
Bioinformatics tools |
tabix(1) |
tabix - Generic indexer for TAB-delimited genome position
files
tabix [-0lf] [-p gff|bed|sam|vcf] [-s
seqCol] [-b begCol] [-e endCol]
[-S lineSkip] [-c metaChar] in.tab.bgz
[region1 [region2 [...]]]
Tabix indexes a TAB-delimited genome position file
in.tab.bgz and creates an index file (in.tab.bgz.tbi or
in.tab.bgz.csi) when region is absent from the command-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". (Coordinates specified in this region
format are 1-based and inclusive.)
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.
The tabix (.tbi) and BAI index formats can handle
individual chromosomes up to 512 Mbp (2^29 bases) in length. If your input
file might contain data lines with begin or end positions greater than that,
you will need to use a CSI index.
Multiple threads can be used for operations except listing of
sequence names.
- -0, --zero-based
- Specify that the position in the data file is 0-based half-open (e.g. UCSC
files) rather than 1-based.
- -b, --begin
INT
- Column of start chromosomal position. [4]
- -c, --comment
CHAR
- Skip lines started with character CHAR. [#]
- -C, --csi
- Produce CSI format index instead of classical tabix or BAI style
indices.
- -e, --end
INT
- Column of end chromosomal position. The end column can be the same as the
start column. [5]
- -f, --force
- Force to overwrite the index file if it is present.
- -m, --min-shift
INT
- Set minimal interval size for CSI indices to 2^INT [14]
- -p, --preset
STR
- Input format for indexing. Valid values are: gff, bed, sam, vcf. 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, --sequence
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]
- -S, --skip-lines
INT
- Skip first INT lines in the data file. [0]
- -h, --print-header
- Print also the header/meta lines.
- -H, --only-header
- Print only the header/meta lines.
- -l, --list-chroms
- List the sequence names stored in the index file.
- -r, --reheader
FILE
- Replace the header with the content of FILE
- -R, --regions
FILE
- Restrict to regions listed in the FILE. The FILE can be BED file (requires
.bed, .bed.gz, .bed.bgz file name extension) or a TAB-delimited file with
CHROM, POS, and, optionally, POS_TO columns, where positions are 1-based
and inclusive. When this option is in use, the input file may not be
sorted.
- -T, --targets
FILE
- Similar to -R but the entire input will be read sequentially and
regions not listed in FILE will be skipped.
- -D
- Do not download the index file before opening it. Valid for remote files
only.
- --cache
INT
- Set the BGZF block cache size to INT megabytes. [10]
This is of most benefit when the -R option is used,
which can cause blocks to be read more than once. Setting the size to 0
will disable the cache.
- --separate-regions
- This option can be used when multiple regions are supplied in the command
line and the user needs to quickly see which file records belong to which
region. For this, a line with the name of the region, preceded by the file
specific comment symbol, is inserted in the output before its
corresponding group of records.
- --verbosity
INT
- Set verbosity of logging messages printed to stderr. The default is 3,
which turns on error and warning messages; 2 reduces warning messages; 1
prints only error messages and 0 is mostly silent. Values higher than 3
produce additional informational and debugging messages.
- -@, --threads INT
- Set number of threads to use for the operation. The default is 0, where no
extra threads are in use.
(grep "^#" in.gff; grep -v "^#" in.gff | sort
-t"`printf '\t'`" -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;
It is straightforward to achieve overlap queries using the
standard B-tree index (with or without binning) implemented in all SQL
databases, 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 efficiently 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.
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.
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