Polygenic score calculation from VCF in Nim.
☆15Nov 22, 2020Updated 5 years ago
Alternatives and similar repositories for nimpress
Users that are interested in nimpress are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- PySeqArray: data manipulation of whole-genome sequencing variants with SeqArray files in Python (pre-release version)☆14Aug 25, 2017Updated 8 years ago
- Alignment and Tabulation of BiSulfite Treated Reads☆16Jan 7, 2014Updated 12 years ago
- Unfazed by genomic variant phasing☆28May 26, 2024Updated 2 years ago
- Detects human contamination in bam files☆16Sep 10, 2020Updated 5 years ago
- Sample Contamination Estimate from VCF☆21Nov 6, 2024Updated last year
- 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.
- ☆15Aug 14, 2020Updated 5 years ago
- Linear-time, low-memory construction of variation graphs☆20Feb 3, 2020Updated 6 years ago
- significance testing over interval overlaps☆30Jul 11, 2020Updated 6 years ago
- IndexTools is a toolkit for extremely fast NGS analysis based on index files.☆17Aug 19, 2022Updated 3 years ago
- Genomic VCF to tab-separated values☆50May 23, 2026Updated 2 months ago
- PRS-on-SPARK☆18Feb 4, 2021Updated 5 years ago
- Infer the age of ancestral nodes in a tree sequence.☆27Jun 30, 2026Updated last month
- Tools for producing pseudo-cgh of next-generation sequencing data☆18Sep 5, 2016Updated 9 years ago
- Divine: Prioritizing Genes for Rare Mendelian Disease in Whole Exome Sequencing Data☆13Apr 18, 2019Updated 7 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.
- Integrative analysis of complex structural variants☆22Sep 7, 2020Updated 5 years ago
- Mutation rate analysis of autosomal loci☆15Jun 25, 2020Updated 6 years ago
- Online material and code base for the article Coordinates and Intervals in Graph Based Reference Genomes☆11May 2, 2017Updated 9 years ago
- collection of small scripts or how-tos that don't fall under a separate project☆21Oct 18, 2017Updated 8 years ago
- ☆14Jul 14, 2026Updated 3 weeks ago
- Teaching modules for Human Genome Variation Lab.☆22Jun 6, 2025Updated last year
- GENI plots to visualise results from genome-wide association studies☆32Oct 14, 2024Updated last year
- Annotate non-coding regulatory vars using our GREEN-DB, prediction scores, conservation and pop AF☆21Jun 13, 2025Updated last year
- Automatised pipeline of ConsensuSV workflow.☆24Aug 23, 2023Updated 2 years ago
- Deploy on Railway without the complexity - Free Credits Offer • AdConnect your repo and Railway handles the rest with instant previews. Quickly provision container image services, databases, and storage volumes.
- The python binding for D4 format☆16Oct 22, 2021Updated 4 years ago
- Spec for R coffee-script☆17Nov 26, 2013Updated 12 years ago
- Detecting NUMTs from WGS☆13Nov 19, 2023Updated 2 years ago
- ☆13May 2, 2018Updated 8 years ago
- Large scale ancestry inference from PCA data☆23May 2, 2023Updated 3 years ago
- ☆13Jun 21, 2017Updated 9 years ago
- ☆10Feb 23, 2022Updated 4 years ago
- Convert 23andMe data to VCFs☆10Aug 8, 2016Updated 10 years ago
- Variant Alert!, a framework to monitor every significant alteration in variant classification and gene-disease association between two ve…☆14Jul 19, 2021Updated 5 years ago
- GPUs on demand by Runpod - Special Offer Available • AdRun AI, ML, and HPC workloads on powerful cloud GPUs—without limits or wasted spend. Deploy GPUs in under a minute and pay by the second.
- Gene lists related to cancer immunotherapy☆14Sep 11, 2024Updated last year
- python stuff I use☆20Feb 16, 2026Updated 5 months ago
- Structural Variation breakpoint discovery via adaptive learning☆17Jul 6, 2023Updated 3 years ago
- ☆12Feb 19, 2017Updated 9 years ago
- Generate an enhanced VCF files from ClinVar XML Full releases☆17Jul 21, 2026Updated 3 weeks ago
- vgraph is a command line application and Python library to compare genetic variants using variant graphs. ``vgraph`` utilizes a graph re…☆43Sep 16, 2021Updated 4 years ago
- SV clustering☆32Jul 5, 2021Updated 5 years ago