Alternatives and similar repositories for biojs-vis-blasterjs:

Users that are interested in biojs-vis-blasterjs are comparing it to the libraries listed below

• YaCui / Biocircos.js
  BioCircos.js - interactive circos for biological data
  ☆24Updated last year
• mskilab-org / gGnome.js
  ☆26Updated 2 years ago
• atc3 / maxquant_linux_guide
  A guide to running MaxQuant in Linux
  ☆32Updated 4 years ago
• dputhier / pygtftk
  A python package and a set of shell commands to handle GTF files
  ☆45Updated 7 months ago
• hammerlab / vcf-annotate-polyphen
  A tool to annotate human VCF files with PolyPhen2 effect measures
  ☆9Updated 2 years ago
• namphuon / ViFi
  Pipeline for identifying viral integration and fusion mRNA reads from NGS data. Manuscript is currently in preparation.
  ☆27Updated 3 years ago
• s-andrews / BamQC
  Mapped QC analysis program
  ☆42Updated 6 years ago
• s-andrews / SeqMonk
  SeqMonk NGS visualisation and analysis tool
  ☆49Updated last week
• nilesh-tawari / ChronQC
  Manuscript describing ChronQC is now available online in Bioinformatics
  ☆17Updated 5 years ago
• vragh / seqvisr
  Biological sequence visualization functions in R
  ☆11Updated 9 months ago
• developerpiru / BEAVR
  BEAVR: A Browser-based tool for the Exploration And Visualization of RNAseq data
  ☆24Updated 2 years ago
• Clinical-Genomics / BALSAMIC
  Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer
  ☆45Updated this week
• bzhanglab / neoflow
  NeoFlow: a proteogenomics pipeline for neoantigen discovery
  ☆22Updated 2 months ago
• Oshlack / MINTIE
  Method for Identifying Novel Transcripts and Isoforms using Equivalence classes, in cancer and rare disease.
  ☆34Updated 6 months ago
• psathyrella / partis
  B- and T-cell receptor sequence annotation, simulation, clonal family and germline inference, and affinity prediction
  ☆57Updated last week
• aryeelab / umi
  Preprocessing tools for unique molecular index (UMI) sequencing reads
  ☆31Updated last year
• sheynkman-lab / Long-Read-Proteogenomics
  A workflow for enhanced protein isoform detection through integration of long-read RNA-seq and mass spectrometry-based proteomics.
  ☆42Updated 2 years ago
• ialbert / bio
  Making bioinformatics fun again
  ☆63Updated 7 months ago
• vpc-ccg / calib
  Calib clusters barcode tagged paired-end reads based on their barcode and sequence similarity.
  ☆38Updated last year
• TrinityCTAT / CTAT-VirusIntegrationFinder
  ☆15Updated last year
• pepkit / geofetch
  Builds a PEP from SRA or GEO accessions
  ☆46Updated 4 months ago
• pinellolab / AmpUMI
  Toolkit for the design and analysis of amplicon sequencing experiments utilizing unique molecular identifiers (UMIs)
  ☆41Updated 8 months ago
• stjude / proteinpaint
  Data visualization and analysis framework focused on phenotype-molecular data integration at cohort level.
  ☆26Updated this week
• enasequence / enaBrowserTools
  A collection of scripts to assist in the retrieval of data from the ENA Browser
  ☆75Updated 9 months ago
• ponnhide / PySanger
  A Python module to analyze Sanger sequencing results.
  ☆21Updated last year
• mikessh / migec
  A RepSeq processing swiss-knife
  ☆41Updated 9 months ago
• saketkc / pyseqlogo
  Python package to plot sequence logos
  ☆29Updated last year
• sbg / smart-variant-filtering
  ☆30Updated 3 years ago
• gdevailly / HeatStarSeq_gh
  A R/shiny web application to browse and compare public RNA-seq / ChIP-seq / CAGE datasets
  ☆18Updated 4 years ago
• xuebingwu / kpLogo
  k-mer probability logo
  ☆11Updated 2 years ago