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pindel
Version:
0.2.5b8
Identifier:
TL_8543fc.f9
Tool
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Overview
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Description
A pattern growth approach to detect break points of large deletions and medium sized insertions from paired end short reads.
Subtools
pindel pindel2vcf
pindel call
Author(s)
Kai Ye
Code Repository
https://github.com/genome/pindel
Links
http://gmt.genome.wustl.edu/packages/pindel/
https://github.com/genome/pindel/issues
https://galaxy.pasteur.fr/tool_runner?tool_id=toolshed.pasteur.fr/repos/fmareuil/pindel/pindel/0.2.5a3
http://gmt.genome.wustl.edu/packages/pindel/
http://gmt.genome.wustl.edu/packages/pindel/user-manual.html
Tags
DNA structural variation
Rare diseases
Sequence motif recognition
Biostars
Pindel too slow. How to speedup
Need help understanding Pindel outputs
What Does Genetype ("0/0", "0/1" Or "1/1") In *.Vcf File Represent?
Filtering Pindel Results
Reducing False Positive Indel Calls From Pindel
Running Pindel On Multiple Samples Produces More Calls Per Sample Than Running Pindel On Single Sample?
PINDEL: Question on Running
Pindel Segmentation Fault Error
Identifying FLT3-ITD with Pindel
filtering pindel results
Extract One-End Mapped Paired-End Reads From Bwa Bam/Sam Files.
SUM_MS field in Pindel, and unique supporting reads discrepancy
Pindel Somatic Calls?
Pindel And Multiple Insert Size Libraries Per Bam File
Pindel output to BED file
pindel _RP and duplictation problem
insertion in pindel _D file?
Somatic indel calling with Pindel
Does Pindel generate genotypes?
Pb to Compile Pindel on MacOs x