bvilhjal / mixmogam

Related projects ⓘ

Alternatives and complementary repositories for mixmogam

• bcbc-group / CyVerese_SNP_calling_webinar
  ☆10Updated 4 years ago
• rwdavies / QUILT
  QUILT: Low coverage whole genome sequence imputation with large reference panels
  ☆53Updated 2 weeks ago
• sanjaynagi / rna-seq-pop
  Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data
  ☆18Updated 3 weeks ago
• Gregor-Mendel-Institute / MultLocMixMod
  An efficient multi-locus mixed-model approach for genome-wide association studies in structured populations
  ☆11Updated 6 years ago
• bartongroup / RATS
  Relative Abundance of Transcripts: An R package for the detection of Differential Transcript isoform Usage.
  ☆32Updated 2 years ago
• tpook92 / HaploBlocker
  R-package: Calculation of haplotype blocks and libraries
  ☆27Updated 8 months ago
• hemstrow / snpR
  ☆28Updated 2 weeks ago
• knausb / vcfR_documentation
  Documentation for vcfR
  ☆10Updated last year
• SexChrLab / XYalign
  ☆23Updated 5 years ago
• kauralasoo / wiggleplotr
  A small R package to make sequencing read coverage plots in R.
  ☆37Updated 2 years ago
• JaeYoonKim72 / GMStool
  ☆16Updated 4 years ago
• adimitromanolakis / sim1000G
  Simulation of rare and common variants based on 1000 genomes data
  ☆18Updated 3 years ago
• schatzlab / scikit-ribo
  Accurate estimation and robust modelling of translation dynamics at codon resolution
  ☆18Updated 7 years ago
• ACAD-UofA / Guide-to-manipulating-PLINK-EIG-and-VCF-files
  A guide to manipulating genotypic data across the common formats: VCF, EIGENSTRAT and PLINK (PACKEDPED) files. Includes how to convert be…
  ☆18Updated last year
• whweve / IntAssoPlot
  ☆15Updated 9 months ago
• AgResearch / KGD
  Kinship (genetic relatedness) using GBS (genotyping-by-sequencing) with Depth adjustment
  ☆21Updated 3 months ago
• healthdisparities / rye
  Large scale ancestry inference from PCA data
  ☆21Updated last year
• ANGSD / NgsRelate
  ☆42Updated 11 months ago
• MerrimanLab / selectionTools
  Pipeline to take VCF through to Selection Analysis.
  ☆58Updated last year
• MorrellLAB / sequence_handling
  A series of scripts to automate sequence workflows
  ☆19Updated 2 months ago
• YaoLab-Bioinfo / intansv
  Integrative analysis of structural variations.
  ☆40Updated 11 months ago
• SFUStatgen / LDheatmap
  ☆15Updated last year
• nf-core / lncpipe
  UNDER DEVELOPMENT--- Analysis of long non-coding RNAs from RNA-seq datasets
  ☆33Updated 6 months ago
• twbattaglia / btools
  A set of R functions that help faciliate a lot of tedious processing
  ☆18Updated 6 years ago
• ramachandran-lab / SWIFr
  Sweep Inference Framework (controlling for correlation)
  ☆28Updated 4 months ago
• ListerLab / TEPID
  Transposable element polymorphism identification
  ☆32Updated 4 years ago
• maxplanck-ie / HiCAssembler
  Software to assemble contigs/scaffolds into chromosomes using Hi-C data
  ☆27Updated last month
• NovembreLab / eems-around-the-world
  Repo to analyze population genetic data with many different methods
  ☆15Updated 5 years ago
• js2264 / tidyCoverage
  ☆20Updated 2 months ago
• AndreasHeger / gat
  Genomic Association Tester
  ☆29Updated last year