testing where SNP are in the humain genom
☆13Oct 24, 2016Updated 10 years ago
Alternatives and similar repositories for snp_location
Users that are interested in snp_location are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Fast, Accurate, and Complete SSR Detection in Genomic Sequences☆11Jun 29, 2020Updated 6 years ago
- Vignettes for Population Genetics in R☆26Aug 11, 2020Updated 6 years ago
- De-novo Assembly Structural Variant Caller☆13Sep 15, 2016Updated 10 years ago
- Retrieve sequences flanked by an arbitrary number of primers from a nucleotide collection.☆11Jun 11, 2021Updated 5 years ago
- A short tutorial to using DL and keras for genomics with sequence data.☆16Dec 3, 2020Updated 5 years ago
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- Mutation rate analysis of autosomal loci☆15Jun 25, 2020Updated 6 years ago
- PySeqArray: data manipulation of whole-genome sequencing variants with SeqArray files in Python (pre-release version)☆14Updated this week
- Long Approximate Matches-based Split Aligner☆13Apr 6, 2017Updated 9 years ago
- Detects human contamination in bam files☆16Sep 10, 2020Updated 6 years ago
- Kneedle algorithm in R -- detecting knees in graphs.☆13Sep 3, 2022Updated 4 years ago
- Fast inference of fine-scale recombination rates based on fused-LASSO☆63Feb 10, 2026Updated 8 months ago
- ☆15Dec 20, 2022Updated 3 years ago
- mist R package files☆10Jul 15, 2026Updated 3 months ago
- DNA kmer operations for nim☆14Apr 24, 2022Updated 4 years ago
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- Toolkit for VNTR genotyping and repeat-pan genome graph construction☆37Aug 18, 2025Updated last year
- Rapid Annotation Transfer Tool☆10May 21, 2025Updated last year
- Pipeline for GTseq genotyping and quality control☆17Jan 30, 2023Updated 3 years ago
- A tool for motif annotation and visualization in tandem repeats.☆15Oct 23, 2026Updated 2 weeks ago
- See all repos served with GitHub pages☆20Nov 9, 2024Updated last year
- RAPTR-SV uses Read Pair and Split Read methods to identify structural variants in paired-end WGS data☆10Aug 18, 2016Updated 10 years ago
- LTR_Finder is an efficient program for finding full-length LTR retrotranspsons in genome sequences.☆51Jan 16, 2024Updated 2 years ago
- ☆12Apr 16, 2024Updated 2 years ago
- ☆20Oct 13, 2014Updated 12 years ago
- 1-Click AI Models by DigitalOcean Gradient • AdDeploy popular AI models on DigitalOcean Gradient GPU virtual machines with just a single click. Zero configuration with optimized deployments.
- ☆11Aug 28, 2026Updated 2 months ago
- Reference genome quality scores☆20Dec 17, 2020Updated 5 years ago
- Tools and Utilities for msmc and msmc2☆51Jan 23, 2026Updated 9 months ago
- Identifying repeats in high-throughput sequencing data☆16Apr 12, 2024Updated 2 years ago
- Pangenome Graph Variation Format (PGVF)☆19Sep 24, 2020Updated 6 years ago
- A standalone end-to-end data analysis pipeline for Duplex Sequencing☆23Oct 25, 2023Updated 3 years ago
- ☆31Mar 5, 2024Updated 2 years ago
- Filtering and profiling of next-generational sequencing data using region-specific rules☆25May 17, 2016Updated 10 years ago
- visual analysis of your VCF files☆40Dec 3, 2022Updated 3 years ago
- Virtual machines for every use case on DigitalOcean • AdGet dependable uptime with 99.99% SLA, simple security tools, and predictable monthly pricing with DigitalOcean's virtual machines, called Droplets.
- R code implementing QTL mapping of physiological, behavioral and gene expression phenotypes in Carworth Farms White (CFW) outbred mice.☆10Aug 24, 2017Updated 9 years ago
- microhaplotype visualizer and analyzer☆23Jun 24, 2021Updated 5 years ago
- This repo contains the knitr code for the paper: Gillespie, C. S., et al, 2010. Analysing yeast time course microarray data using BioCond…☆12Jan 25, 2016Updated 10 years ago
- ☆27Aug 8, 2024Updated 2 years ago
- alignment and assembly free☆14May 29, 2023Updated 3 years ago
- The snakemake workflow for whole-exome sequencing analysis and generating vcf files☆11Dec 17, 2022Updated 3 years ago
- Work from the book 'Advanced Python for Biologists'☆15Sep 12, 2018Updated 8 years ago