☆30Jul 10, 2019Updated 7 years ago
Alternatives and similar repositories for XYalign
Users that are interested in XYalign are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Identifying, understanding, and correcting technical biases on the sex chromosomes in next-generation sequencing data☆23Apr 11, 2019Updated 7 years ago
- Somatic (mosaic) SNV caller for 10X Genomics data using random forest classification and feature-based filters☆23Apr 1, 2019Updated 7 years ago
- A simple tool to fix PacBio fasta/q that was not properly split into subreads☆16Jun 10, 2021Updated 5 years ago
- A filter algorithm with program to filter an alignment or mapping file☆12May 15, 2025Updated last year
- plot genome alignment synteny☆20May 25, 2020Updated 6 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.
- Lossless VCF compression☆22Mar 4, 2022Updated 4 years ago
- ☆12Jun 7, 2024Updated 2 years ago
- ☆11Nov 21, 2025Updated 8 months ago
- pythonic wrapper for htslib☆24Aug 8, 2017Updated 9 years ago
- Annotate Olfactory receptor CDS from genome☆11Apr 29, 2023Updated 3 years ago
- Code repository for the T2T-Y paper☆24Jul 11, 2023Updated 3 years ago
- A tool for sniffing out the differences in vari-Ants☆45Apr 7, 2026Updated 4 months ago
- ☆32Jan 5, 2023Updated 3 years ago
- Clinical interpretation of somatic mutations in cancer☆53Feb 20, 2025Updated last year
- 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.
- ☆11May 21, 2024Updated 2 years ago
- Bayesian analysis of MPRA and other high-throughput genomic assays☆10Jul 27, 2020Updated 6 years ago
- Align subreads to ccs reads☆14Jun 11, 2025Updated last year
- Concordance and contamination estimator for tumor–normal pairs☆60Oct 22, 2024Updated last year
- Structural Variation breakpoint discovery via adaptive learning☆17Jul 6, 2023Updated 3 years ago
- Location of public benchmarking; primarily final results☆18Feb 17, 2025Updated last year
- The complete sequence of a Chinese individual☆14Oct 8, 2024Updated last year
- Calculate Hybrid Index and Heterozygosity from SNP data☆17Sep 2, 2025Updated 11 months ago
- ChromeQC: Summarize sequencing library quality of 10x Genomics Chromium linked reads☆15Apr 30, 2019Updated 7 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.
- ☆10Jun 13, 2020Updated 6 years ago
- Github Gists from the command line. On MAC OSX, it (will be) an Alfred Workflow!☆11Dec 20, 2020Updated 5 years ago
- a tool to evaluate long-read error correction mainly with PacBio High-Fidelity Reads (HiFi reads).☆20Dec 5, 2023Updated 2 years ago
- beRi "beri environments for R installations" is an R environment, R installation, and R package management system for R☆14Dec 23, 2025Updated 7 months ago
- Figures for the CHM13 T2T SD paper.☆12Sep 12, 2021Updated 4 years ago
- A statistical framework for reference-free inference of archaic local ancestry☆15Nov 8, 2019Updated 6 years ago
- BAMixChecker: A fast and efficient tool for sample matching checkup☆16Jun 12, 2022Updated 4 years ago
- Workshop: Using R/tidyverse to analyze & visualize gapminder/processed transcriptomics data!☆13Sep 12, 2025Updated 10 months ago
- de novo targeted gene assembly☆22Apr 16, 2021Updated 5 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.
- Pipeline for structural variant image curation and analysis.☆49Dec 5, 2021Updated 4 years ago
- Sample an approximate number of reads from a fastq file without reading the entire file☆11Jun 20, 2017Updated 9 years ago
- Multi-sample genome coverage viewer to observe large, coverage-based anomalies alongside annotations and sample metadata☆58Feb 17, 2022Updated 4 years ago
- ☆32Jun 18, 2026Updated last month
- Split a BAM file by haplotype support☆16Dec 13, 2017Updated 8 years ago
- This is the GitHub repository for our benchmarking study "Benchmarking of computational error-correction methods for next-generation sequ…☆12Mar 13, 2020Updated 6 years ago
- IgSimulator is a versatile tool for simulation of immunoglobulin repertoire☆12Nov 25, 2016Updated 9 years ago