Entering edit mode
20 months ago
drkuldeepbiotech
•
0
$ gmap_build -D:\btau8refflat.gtf
Unknown option: D:btau8refflat.gtf
-k flag not specified, so building main hash table with default 15-mers
-j flag not specified, so building regional hash tables with default 6-mers
gmap_build: Builds a gmap database for a genome to be used by GMAP or GSNAP.
Part of GMAP package, version 2021-12-17.
Usage: gmap_build [options...] -d <genome> [-c <transcriptome> -T <transcript_fasta>] <genome_fasta_files>
You are free to name <genome> and <transcriptome> as you wish. You
will use the same names when performing alignments subsequently using
GMAP or GSNAP.
Note: If adding a transcriptome to an existing genome, then there is
no need to specify the genome_fasta_files. This way you can add
transcriptome information to an existing genome database.
Options:
-D, --dir=STRING Destination directory for installation (defaults to gmapdb
directory specified at configure time)
-d, --genomedb=STRING Genome name (required)
-n, --names=STRING Substitute names for contigs, provided in a file.
The file can have two formats:
1. A file with one column per line, with each line
corresponding to a FASTA file, in the order given to
gmap_build. The chromosome name for each FASTA file will
be replaced with the desired chromosome name in the file.
Every chromosome in the FASTA must have a corresponding line
in the file. This is useful if you want to rename chromosomes
with a systematic numbering pattern.
2. A file with two columns per line, separated by white
space. In each line, the original FASTA chromosome name
should be in column 1 and the desired chromosome name
will be in column 2.
The meaning of file format 2 depends on whether
--limit-to-names is specified. If so, the genome build will
be limited to those chromosomes in this file. Otherwise,
all chromosomes in the FASTA file will be included,
but only those chromosomes in this file will be re-named, which
provides an easy way to change just a few chromosome names.
This file can be combined with the --sort=names option, in
which the order of chromosomes is that given in the file. In
this case, every chromosome must be listed in the file, and
for chromosome names that should not be changed, column 2 can
be blank (or the same as column 1). The option of a blank
column 2 is allowed only when specifying --sort=names,
because otherwise, the program cannot distinguish between a
1-column and 2-column names file.
-L, --limit-to-names Determines whether to limit the genome build to the lines listed
in the --names file. You can limit a genome build to certain
chromosomes with this option, plus a --names file that either
renames chromosomes, or lists the same names in both columns for
the desired chromosomes.
-k, --kmer=INT k-mer value for genomic index (allowed: 15 or less, default is 15)
-q INT sampling interval for genomoe (allowed: 1-3, default 3)
-s, --sort=STRING Sort chromosomes using given method:
none - use chromosomes as found in FASTA file(s) (default)
alpha - sort chromosomes alphabetically (chr10 before chr 1)
numeric-alpha - chr1, chr1U, chr2, chrM, chrU, chrX, chrY
chrom - chr1, chr2, chrM, chrX, chrY, chr1U, chrU
names - sort chromosomes based on file provided to --names flag
-g, --gunzip Files are gzipped, so need to gunzip each file first
-E, --fasta-pipe=STRING Interpret argument as a command, instead of a list of FASTA files
-Q, --fastq Files are in FASTQ format
-R, --revcomp Reverse complement all contigs
-w INT Wait (sleep) this many seconds after each step (default 2)
-o, --circular=STRING Circular chromosomes (either a list of chromosomes separated
by a comma, or a filename containing circular chromosomes,
one per line). If you use the --names feature, then you
should use the substitute name of the chromosome, not the
original name, for this option. (NOTE: This behavior is different
from previous versions, and starts with version 2020-10-20.)
-2, --altscaffold=STRING File with alt scaffold info, listing alternate scaffolds,
one per line, tab-delimited, with the following fields:
(1) alt_scaf_acc, (2) parent_name, (3) orientation,
(4) alt_scaf_start, (5) alt_scaf_stop, (6) parent_start, (7) parent_end.
-e, --nmessages=INT Maximum number of messages (warnings, contig reports) to report (default 50)
Options for older genome formats: -M, --mdflag=STRING Use MD file from NCBI for mapping contigs to chromosomal coordinates
-C, --contigs-are-mapped Find a chromosomal region in each FASTA header line.
Useful for contigs that have been mapped
to chromosomal coordinates. Ignored if the --mdflag is provided.
Options for transcriptome-guided alignment: -c, --transcriptomedb=STRING Transcriptome name
-T, --transcripts=FILE FASTA file containing transcripts (required if specifying
--transcriptomedb)
-t, --nthreads=INT Number of threads for GMAP alignment of transcripts to genome
(default 8)
Must specify genome database name with -d flag. at /usr/bin/gmap_build line 69.
No need to paste that all. A command line, the error and a wrotten sentence wouldn've been better. Are you on Windows?
yes i am on window
This is a permission error unrelated to BWA. Your environment doesn't have the permission to write.
How can i Resolve it
learn to read the error messages:
it tells you that you have not defined a cache directory and it picked one by default, but later it turns out it can't write there