Alternatives and similar repositories for dotnetbio.github.io

Users that are interested in dotnetbio.github.io are comparing it to the libraries listed below

• dotnetbio / bio
  Bioinformatics library for .NET
  ☆156Updated 8 years ago
• arklumpus / TreeViewer
  Cross-platform software to draw phylogenetic trees
  ☆234Updated 4 months ago
• austin-putz / BLUPF90
  Random stuff for BLUPF90 programs
  ☆17Updated 2 years ago
• OpenGene / CfdnaPattern
  Pattern Recognition for Cell-free DNA
  ☆59Updated 7 years ago
• MatthewHiggins2017 / bioconda-PrimedRPA
  ☆24Updated 2 years ago
• SMRUCC / GCModeller
  GCModeller: genomics CAD(Computer Assistant Design) Modeller system in .NET language
  ☆38Updated this week
• tiramisutes / qPCR-Pipeline
  Auto-analysis for Real-Time PCR (qPCR) data
  ☆41Updated 2 years ago
• seppinho / haplogrep-cmd
  HaploGrep - mtDNA haplogroup classification. Supporting rCRS and RSRS.
  ☆77Updated 2 years ago
• gear-genomics / indigo
  Indigo: SNV and InDel Discovery in Chromatogram traces obtained from Sanger sequencing of PCR products
  ☆36Updated 2 months ago
• Trinotate / Trinotate
  Trinotate source code
  ☆84Updated last year
• 4dn-dcic / pairix
  1D/2D indexing and querying on bgzipped text file with a pair of genomic coordinates
  ☆92Updated last year
• OpenGene / MrBam
  Query Mutated Reads from a Bam
  ☆26Updated 7 years ago
• nf-core / raredisease
  Call and score variants from WGS/WES of rare disease patients.
  ☆112Updated this week
• shenwei356 / bio_scripts
  Practical, reusable scripts for bioinformatics
  ☆102Updated 6 years ago
• stamatak / RAxML-Light-1.0.5
  ☆17Updated 13 years ago
• mdshw5 / fastqp
  Simple FASTQ quality assessment using Python
  ☆109Updated 4 years ago
• WGLab / biocluster
  Tutorial on building a computing cluster for bioinformatics
  ☆88Updated 2 years ago
• hbc / bcbioRNASeq
  R package for bcbio RNA-seq analysis.
  ☆63Updated last year
• umd-byob / presentations
  Bring Your Own Bioinformatics
  ☆27Updated 9 years ago
• PacificBiosciences / barcoding
  Lima - Demultiplex Barcoded PacBio Samples
  ☆68Updated 8 months ago
• davetang / learning_vcf_file
  Learning the Variant Call Format
  ☆148Updated 6 months ago
• Illumina / canvas
  Canvas - Copy number variant (CNV) calling from DNA sequencing data
  ☆128Updated 6 years ago
• Czh3 / NGSTools
  Next-Generation Sequencing(NGS) toolkits.
  ☆48Updated 9 years ago
• nextflow-io / crg-course-nov16
  Nextflow + Docker tutorial material
  ☆25Updated 8 years ago
• Illumina / interop
  C++ Library to parse Illumina InterOp files
  ☆80Updated last month
• brwnj / bcl2fastq
  NextSeq specific bcl2fastq2 wrapper.
  ☆55Updated 4 years ago
• OpenGene / GeneFuse
  Gene fusion detection and visualization
  ☆131Updated 3 years ago
• OpenGene / MutScan
  Detect and visualize target mutations by scanning FastQ files directly
  ☆157Updated 3 years ago
• NYU-BFX / hic-bench
  A set of pipelines for Hi-C and ChIP-Seq analysis.
  ☆48Updated last year
• NCGAS / de-novo-transcriptome-assembly-pipeline
  Combined de novo transcriptome assembly - multiple assemblers - multiple parameters
  ☆18Updated 4 years ago