Alternatives and similar repositories for juxtapose

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

• zd105 / AllEnricher
  A comprehensive gene set function enrichment tool for multiple species.
  ☆13Updated 5 years ago
• yuansliu / minirmd
  ☆12Updated 2 years ago
• jhhung / EARRINGS
  EARRINGS: An efficient and ingenious adapter removal design for large-scale NGS meta-analyses
  ☆9Updated 2 months ago
• salbrec / seqQscorer
  ☆22Updated 2 months ago
• Pandaman-Ryan / AgentBind
  ☆13Updated 10 months ago
• comprna / R2Dtool
  Analyse RNA feature distributions.
  ☆16Updated 7 months ago
• nch-igm / snvstory
  Rapid and accurate ancestry inference using SNVs.
  ☆19Updated last week
• czhu / FulQuant
  FulQuant pipeline to identify and quantify transcript isoforms based on Nanopore long-read data
  ☆9Updated 2 years ago
• Kari-Genomics-Lab / iDeLUCS
  Source code for iDeLUCS. An interactive deep-learning based tool for clustering of genomic sequences
  ☆14Updated last year
• microsoft / BindVAE
  Variational Auto Encoders for learning binding signatures of transcription factors
  ☆12Updated last year
• kuijjerlab / PySNAIL
  Smooth-quantile Normalization Adaptation for Inference of co-expression Links
  ☆16Updated 2 years ago
• Gregor-Mendel-Institute / bookend
  End-guided RNA assembler
  ☆15Updated 3 months ago
• pachterlab / qcbc
  ☆20Updated last month
• qm2 / gpress
  This is the GPress, a framework for querying GTF, GFF3 and expression files in a compressed form.
  ☆12Updated last year
• fedarko / strainFlye
  Pipeline for analyzing (rare) mutations in metagenome-assembled genomes
  ☆11Updated 3 months ago
• ay-lab / ExTraMapper
  ExTraMapper is a tool to find Exon and Transcript-level Mappings of a given pair of orthologous genes between two organisms using sequenc…
  ☆11Updated 3 years ago
• splicebox / MntJULiP
  Comprehensive and scalable differential splicing analyses
  ☆17Updated 4 months ago
• XPRESSyourself / XPRESSpipe
  An alignment and analysis pipeline for Ribosome Profiling and RNA-seq data
  ☆13Updated last year
• KHP-Informatics / DNAscanv2
  DNAscan2 is a fast and efficient bioinformatics pipeline that allows for the analysis of DNA Next Generation sequencing data, requiring v…
  ☆14Updated last year
• matsengrp / phip-flow
  A Nextflow pipeline to align, merge, and organize large PhIP-Seq datasets
  ☆13Updated 5 months ago
• slncky / slncky
  slncky is a tool for lncRNA discovery from RNA-Seq data. slncky filters a high-quality set of noncoding transcripts, discovers lncRNA or…
  ☆11Updated 4 years ago
• ImperialCardioGenetics / uORFs
  ☆18Updated 5 years ago
• xia-lab / Seq2Fun
  ☆16Updated last week
• lauringlab / variant_pipeline
  Work on the variant_pipeline and initial r analysis used in calling variants from NGS data
  ☆9Updated 6 years ago
• nf-core / kmermaid
  k-mer similarity analysis pipeline
  ☆21Updated last week
• BIGslu / kimma
  Kinship In Mixed Model Analysis of RNA-seq
  ☆13Updated 3 months ago
• ngs-docs / 2021-GGG298
  Winter 2021, GGG 298 - Tools for Data Intensive Research - UC Davis
  ☆12Updated 4 years ago
• quinlan-lab / pathoscore
  pathoscore evaluates variant pathogenicity tools and scores.
  ☆21Updated 3 years ago
• naznoosh / MSA
  ☆9Updated 4 years ago
• WGLab / AmpBinner
  A barcode demultiplexer for Oxford Nanopore long-read amplicon sequencing data
  ☆10Updated 7 months ago