Alternatives and similar repositories for I2P4B

Users that are interested in I2P4B are comparing it to the libraries listed below

• wksofia / wgs_pipeline
  wgs_pipeline
  ☆18Updated 12 years ago
• sebhtml / FastDemultiplexer
  A sequence demultiplexer for the Illumina HiSeq technology
  ☆21Updated 12 years ago
• YangLab / CIRCexplorer
  A combined strategy to identify circular RNAs (circRNAs and ciRNAs) (Zhang et al., Complementary Sequence-Mediated Exon Circularization, …
  ☆62Updated 6 years ago
• genome / somatic-sniper
  A tool to call somatic single nucleotide variants.
  ☆41Updated 10 years ago
• gt1 / biobambam
  Tools for bam file processing
  ☆55Updated 10 years ago
• smithlabcode / walt
  WALT is a read mapping program for bisulfite sequencing DNA methylation studies.
  ☆17Updated 3 years ago
• openbiox / wiki
  Let's get started!
  ☆15Updated 6 years ago
• wegene-llc / radmixture
  an R package for ancestry analysis
  ☆37Updated 7 years ago
• boutroslab / cld
  A software for the multispecies design of CRISPR/Cas9 libraries
  ☆36Updated 3 years ago
• daler / metaseq
  Framework for integrated analysis and plotting of ChIP/RIP/RNA/*-seq data
  ☆87Updated 5 years ago
• ngsutils / ngsutils
  Tools for next-generation sequencing analysis
  ☆89Updated 6 years ago
• kingsfordgroup / sailfish
  Rapid Mapping-based Isoform Quantification from RNA-Seq Reads
  ☆127Updated 3 years ago
• genome-in-a-bottle / giab_data_analysis
  This repository contains information about ongoing analysis performed by GIAB
  ☆14Updated 6 years ago
• openbiox / openbiox-Translation
  openbiox 翻译计划
  ☆16Updated 6 years ago
• homologus / Pandoras-Toolbox-for-Bioinformatics
  A collection of well-known bioinformatics programs.
  ☆25Updated 10 years ago
• wanpinglee / MOSAIK
  reference-guided aligner for next-generation sequencing technologies
  ☆57Updated 9 years ago
• mdshw5 / fastqp
  Simple FASTQ quality assessment using Python
  ☆109Updated 4 years ago
• soccin / BIC-variants_pipeline
  BIC@MSKCC Variants Pipeline
  ☆23Updated 2 years ago
• broadinstitute / oncotator
  ☆69Updated 3 years ago
• bioinform / rnacocktail
  ☆89Updated 5 years ago
• andrewjesaitis / variant-annotation-comparison-2017
  Work supporting the comparison of SnpEff and VEP effect prediction and HGVS identifiers
  ☆11Updated 8 years ago
• EarlhamInst / 361Division
  361 Division - Scientific Training, Education and Learning
  ☆28Updated 5 years ago
• slowkow / picardmetrics
  Run Picard on BAM files and collate 90 metrics into one file.
  ☆40Updated 8 years ago
• ShujiaHuang / cmdbtools
  Command line tools for CMDB varaints browser
  ☆23Updated last year
• PapenfussLab / socrates
  ☆16Updated 9 years ago
• chrisamiller / readDepth
  R package for inferring copy number from read depth
  ☆32Updated 3 years ago
• sanger-cellular-informatics / CRISPR-Analyser
  C++ package for analysing CRISPR off targets
  ☆21Updated 4 years ago
• rhshah / IMPACT-Pipeline
  Framework to process and call somatic variation from NGS dataset generated using MSK-IMPACT assay
  ☆57Updated 4 years ago
• yuchaojiang / Canopy
  Accessing Intra-Tumor Heterogeneity and Tracking Longitudinal and Spatial Clonal Evolutionary History by Next-Generation Sequencing.
  ☆70Updated 4 years ago
• bjpop / methpat
  A program for summarising CpG methylation patterns
  ☆20Updated 9 years ago