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pindel

Version:
0.2.5b8
Identifier: TL_8543fc.f9
Tool
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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
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