conv_gtf_to_bed - legacy script for invoking the PALEOMIX command "gtf_to_bed"
Contents
Description
The PALEOMIX pipelines are a set of pipelines and tools designed to aid the rapid processing of High-
Throughput Sequencing (HTS) data: The BAM pipeline processes de-multiplexed reads from one or more
samples, through sequence processing and alignment, to generate BAM alignment files useful in downstream
analyses; the Phylogenetic pipeline carries out genotyping and phylogenetic inference on BAM alignment
files, either produced using the BAM pipeline or generated elsewhere; and the Zonkey pipeline carries out
a suite of analyses on low coverage equine alignments, in order to detect the presence of F1-hybrids in
archaeological assemblages. In addition, PALEOMIX aids in metagenomic analysis of the extracts.
The pipelines have been designed with ancient DNA (aDNA) in mind, and includes several features
especially useful for the analyses of ancient samples, but can all be for the processing of modern
samples, in order to ensure consistent data processing.
conv_gtf_to_bed is a legacy script for invoking the paleomix(1) command "gtf_to_bed"
Name
conv_gtf_to_bed - legacy script for invoking the PALEOMIX command "gtf_to_bed"
Options
positionalarguments:
INPUT.gtf
Input file in GTF format.
OUTPUT_PREFIX
Prefix of output files.
SCAFFOLDS
Mapping of scaffolds to contig positions; e.g. mapping individual Un* scaffolds onto chrUn.
optionalarguments:-h, --help
show this help message and exit
--keep-all-transcripts
Include all transcripts in the output BED files, not just the longest transcript of each gene
[default: off]
--keep-malformed-proteins
Include transcripts of protein-coding in the output, even if the the length of the CDS is not
divisible by 3 [default: off]
--contig-prefix CONTIG_PREFIX
Add prefix to contig names (e.g. 'chr') [default: no prefix].
See Also
paleomix(1)
Synopsis
paleomixgtf_to_bed [options] in.gtf out_prefix [in.scaffolds]
