Parse Copy Number Variation from Array and Sequencing
☆19Dec 1, 2023Updated 2 years ago
Alternatives and similar repositories for ParseCNV2
Users that are interested in ParseCNV2 are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Calculates the probability of a haplotype given a population reference panel☆12Dec 9, 2024Updated last year
- An efficient tool for cross-population fixation index estimation on variant call format files☆11Mar 1, 2026Updated 2 months ago
- Genomic Annotation in Livestock for positional candidate LOci☆13Feb 26, 2021Updated 5 years ago
- an R based software package that makes polygenic traits prediction using gradient boosted and LD adjusted gene score weights.☆10Apr 9, 2019Updated 7 years ago
- Chromosome Scale Assembler: A high-throughput chromosome scale genome assembly pipeline for vertebrate genomes☆10Oct 16, 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.
- Next Generation Genomic Prediction Tools☆10Updated this week
- ☆19Nov 22, 2022Updated 3 years ago
- MP-EST estimates species trees from a set of gene trees by maximizing a pseudo-likelihood function☆12Oct 31, 2025Updated 6 months ago
- ☆11May 21, 2024Updated last year
- Toolkit for genome-wide analysis of tandem repeats☆62Apr 27, 2026Updated last week
- use paired-end transcriptome reads to scaffold genomes☆11May 30, 2019Updated 6 years ago
- VcfExplorer regroups several programs which principal aims are to map DNA and RNAseq data onto reference genome sequence, perform variant…☆15Apr 15, 2026Updated 3 weeks ago
- Deleterious mutation prediction pipeline☆13Dec 16, 2024Updated last year
- Documentation for the Helium pedigree visualization software☆17Apr 3, 2024Updated 2 years ago
- Deploy open-source AI quickly and easily - Special Bonus Offer • AdRunpod Hub is built for open source. One-click deployment and autoscaling endpoints without provisioning your own infrastructure.
- Copy number vaiation detection from SNP arrays☆97May 19, 2024Updated last year
- Evaluation of phasing performance☆23Mar 6, 2018Updated 8 years ago
- Instruction and scripts for reconstructing ancestral genome from pairwise syntenic blocks using MLGO☆13Oct 30, 2018Updated 7 years ago
- Heritability, genetic correlation and functional enrichment estimation for case-control studies☆20Nov 26, 2023Updated 2 years ago
- Stochastic-Lanczos-Expedited Mixed Models☆10Dec 10, 2025Updated 5 months ago
- Aggregation and analyses of rare CNVs across diseases☆15Jan 25, 2023Updated 3 years ago
- Clann: Investigation of phylogenomic signal using supertrees☆18Apr 21, 2026Updated 2 weeks ago
- ☆10Oct 30, 2023Updated 2 years ago
- Structural Variation breakpoint discovery via adaptive learning☆17Jul 6, 2023Updated 2 years ago
- Bare Metal GPUs on DigitalOcean Gradient AI • AdPurpose-built for serious AI teams training foundational models, running large-scale inference, and pushing the boundaries of what's possible.
- ☆17Oct 21, 2024Updated last year
- ☆11Jun 13, 2024Updated last year
- A framework for network analysis and display of SNPs☆20Oct 31, 2016Updated 9 years ago
- Code to reproduce analysis and figures for 'Genetic mapping of etiologic brain cell types for obesity' (Timshel, eLife 2020)☆14May 20, 2021Updated 4 years ago
- Exome Copy Number Variation Polisher via Deep Learning☆18Jun 1, 2020Updated 5 years ago
- Efficient Local Ancestry Inference☆17Nov 10, 2025Updated 6 months ago
- The MafFilter genome alignment processor☆19Apr 10, 2026Updated last month
- Cell Heterogeneity Accounted cLonal Methylation (CHALM)☆10Jul 6, 2021Updated 4 years ago
- Plot CNV data with a genome viewer in R☆15Apr 5, 2017Updated 9 years ago
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting for WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Deploy in minutes on Cloudways by DigitalOcean.
- ☆11Mar 16, 2022Updated 4 years ago
- Application of the Simple Sum method for testing co-localization of GWAS with any other SNP-level data (e.g. eQTL data)☆10Jan 26, 2026Updated 3 months ago
- R functions related to pedigrees☆14Sep 29, 2025Updated 7 months ago
- Summary-level Unified Method for Modeling Integrated Transcriptome☆10Jun 27, 2023Updated 2 years ago
- ☆33Feb 24, 2026Updated 2 months ago
- ☆19Sep 20, 2020Updated 5 years ago
- Scripts and utilities for analyzing tandem repeats (TRs).☆45Apr 15, 2026Updated 3 weeks ago