sailalithabollepalli / EpiSmokErView external linksLinks
Epigenetic Smoking status Estimator
☆11Nov 24, 2020Updated 5 years ago
Alternatives and similar repositories for EpiSmokEr
Users that are interested in EpiSmokEr are comparing it to the libraries listed below
Sorting:
- A new extended cell deconvolution for peripheral blood☆18Feb 28, 2025Updated 11 months ago
- Community-maintained list of resources that the CI4CC organization and the larger cancer informatics community have found useful or are d…☆22Sep 24, 2018Updated 7 years ago
- A cross-package Bioconductor workflow for analysing methylation array data☆11Mar 31, 2017Updated 8 years ago
- A tool set to assess the quality of the per read phasing and reduce the errors.☆13Jun 25, 2020Updated 5 years ago
- Structural Variation breakpoint discovery via adaptive learning☆16Jul 6, 2023Updated 2 years ago
- Code to implement the DunedinPACE scoring algorithm in Illumina 450k or EPIC array data☆46Jun 6, 2025Updated 8 months ago
- Plot CNV data with a genome viewer in R☆15Apr 5, 2017Updated 8 years ago
- CAVA (Clinical Annotation of VAriants)☆14Sep 28, 2018Updated 7 years ago
- 🍪 SEnsible Step-wise Analysis of DNA MEthylation BeadChips☆80Feb 6, 2026Updated last week
- A series of tools and pipelines for genotyping MHC / HLA genes and alleles using SMRT Sequencing☆22Aug 29, 2016Updated 9 years ago
- Lossless VCF compression☆21Mar 4, 2022Updated 3 years ago
- Predict epigenetic age from DNA methylation data☆68Nov 26, 2025Updated 2 months ago
- Code for the calculation and implementation of the PC Based epigenetic clocks☆60Dec 9, 2025Updated 2 months ago
- Tools for finding mobile element insertions from single-end datasets☆24Dec 14, 2019Updated 6 years ago
- Detecting intron retention from RNA-Seq experiments☆55Jul 17, 2024Updated last year
- A BioWDL variantcalling pipeline for germline DNA data. Starting with FASTQ files to produce VCF files. Category:Multi-Sample☆26May 4, 2023Updated 2 years ago
- A Practical (And Opinionated) Guide To Analyzing 450K Data☆35Oct 2, 2014Updated 11 years ago
- ☆26Jun 4, 2025Updated 8 months ago
- Seeking information like heteroplasmy, structure variants, etc. on Mitochondrial genome from next generation sequencing☆41Dec 11, 2018Updated 7 years ago
- ☆35Mar 2, 2021Updated 4 years ago
- Preprocessing methylation pipeline, written in python. Easy to use and highly parallelized.☆36Feb 11, 2020Updated 6 years ago
- Ready-to-go Parquet-formatted public 'omics datasets☆30Nov 2, 2015Updated 10 years ago
- Clonal reconstruction from HTS data☆10Oct 27, 2021Updated 4 years ago
- A machine learning tool to predict tandem repeat pathogenicity☆12Jan 2, 2024Updated 2 years ago
- collection of interviews made by constantvzw.org☆11Apr 11, 2015Updated 10 years ago
- mity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data☆40Sep 8, 2025Updated 5 months ago
- Deep Variant as a Nextflow pipeline☆30Jul 24, 2020Updated 5 years ago
- Estimate a suite of normalizing transformations, including a new adaptation of a technique based on ranks which can guarantee normally di…☆41Nov 29, 2025Updated 2 months ago
- A tool for visualizing alignments of reads in regions containing tandem repeats☆90Dec 19, 2023Updated 2 years ago
- dbVar☆40Sep 13, 2022Updated 3 years ago
- Harnessing FABRIC for Scalable Human Genome Sequence Analysis☆12Feb 7, 2026Updated last week
- Divine: Prioritizing Genes for Rare Mendelian Disease in Whole Exome Sequencing Data☆13Apr 18, 2019Updated 6 years ago
- ☆14Mar 26, 2024Updated last year
- Bioinformatics Training Platform (BTP) Workshop: Introduction to NGS☆10Oct 31, 2018Updated 7 years ago
- RStudio Cloud ☁️ resources to accompany tidymodels.org☆12Oct 28, 2021Updated 4 years ago
- ☆10May 17, 2017Updated 8 years ago
- ☆16Jul 5, 2019Updated 6 years ago
- A versatile method for systematic identification of differential RNA splicing across platforms☆15Jan 15, 2026Updated last month
- HIVID2 is a tool for detecting virus integration events in the host genome.☆12Oct 1, 2023Updated 2 years ago