EpigenomeClock / MouseEpigeneticClockLinks
☆13Updated 6 years ago
Alternatives and similar repositories for MouseEpigeneticClock
Users that are interested in MouseEpigeneticClock are comparing it to the libraries listed below
Sorting:
- structure detection program☆18Updated last year
- Abismal is a mapper of FASTQ bisulfite-converted short reads (between 50 and 1000 bases) to a FASTA reference genome.☆20Updated last week
- A toolset for handling sequencing data with unique molecular identifiers (UMIs)☆17Updated 7 years ago
- ☆18Updated 4 years ago
- Workflow for Sequenza, cellularity and ploidy☆26Updated 5 months ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 3 years ago
- Long read to rMATS☆32Updated 2 years ago
- Calib clusters barcode tagged paired-end reads based on their barcode and sequence similarity.☆40Updated 2 years ago
- This script use to analyze the immune repertoire sequenced by high throughtput sequencing☆27Updated 4 years ago
- Pipeline for identifying viral integration and fusion mRNA reads from NGS data. Manuscript is currently in preparation.☆30Updated 4 years ago
- MethGo: a comprehensive tool for analyzing whole-genome bisulfite sequencing data☆21Updated 8 years ago
- Comprehensive Human Expressed SequenceS☆19Updated 6 months ago
- miRge - microRNA alignment software for small RNA-seq data, now at v2.0☆28Updated 3 years ago
- Millefy: Genome browser-like visualization of single-cell RNA-seq dataset☆29Updated 6 years ago
- NeoFuse is a user-friendly pipeline for the prediction of fusion neoantigens from tumor RNA-seq data.☆20Updated 3 years ago
- BANDITS: Bayesian ANalysis of DIfferenTial Splicing☆19Updated 4 months ago
- Detection and Visualization of Exon-Level Copy Number Variants in Targeted Next Generation Sequencing Data☆18Updated 4 years ago
- Reconstructs complex variation using Bionano optical mapping data and breakpoint graph data☆19Updated 2 years ago
- Predicting TF sequence-specificity similarity with weighted alignments☆13Updated 6 years ago
- Versatile FASTA/FASTQ demultiplexer.☆33Updated last year
- A Computational Workflow for Designing Libraries of sgRNAs for CRISPR-Mediated Base Editing, and much more☆19Updated last year
- Code to reproduce "Detecting liver cancer using cell-free DNA fragmentomes☆11Updated 3 years ago
- ☆17Updated last year
- FunctionaL Omics Processing platform☆13Updated last year
- ☆11Updated 2 years ago
- predicts neoepitopes from phased somatic mutations detected using tumor/normal DNA-seq data☆27Updated 2 years ago
- ☆13Updated 3 years ago
- A p-value-free method for controlling false discovery rates in high-throughput biological data with two conditions☆41Updated 3 years ago
- alternative splicing analysis pipeline☆20Updated 4 years ago
- Combined mutation recurrence and functional impact to identify coding and non-coding cancer drivers☆15Updated 7 years ago