hawkjo / freebarcodesLinks
FREE Divergence Error-Correcting DNA Barcodes
☆27Updated 6 months ago
Alternatives and similar repositories for freebarcodes
Users that are interested in freebarcodes are comparing it to the libraries listed below
Sorting:
- Code from "Deep Learning Of The Regulatory Grammar Of Yeast 5′ Untranslated Regions From 500,000 Random Sequences"☆15Updated 7 years ago
- Comparison of Adaptive Immune Receptor Repertoires☆27Updated 7 months ago
- Predicting gene expression levels from genomic sequences☆54Updated 5 years ago
- Tool package to perform in-silico CRISPR analysis and assessment☆30Updated last year
- B- and T-cell receptor sequence annotation, simulation, clonal family and germline inference, and affinity prediction☆59Updated last week
- off-targeting assessment of Cas9 gRNAs☆13Updated 4 years ago
- RNA structure probing and post-transcriptional modifications mapping high-throughput data analysis☆40Updated last month
- Python package to plot sequence logos☆29Updated last year
- Bayesian enrichment estimation in R☆11Updated 3 years ago
- Efficient algorithms for designing orthogonal DNA sequence libraries☆13Updated 10 months ago
- Python port of the R Bioconductor `seqLogo` package☆34Updated last year
- MAVE-NN: genotype-phenotype maps from multiplex assays of variant effect☆28Updated last week
- MetaLogo: a heterogeneity-aware sequence logo generator and aligner☆21Updated 2 years ago
- Toolkit for the design and analysis of amplicon sequencing experiments utilizing unique molecular identifiers (UMIs)☆42Updated last year
- Saluki, a method to predict mRNA half-lives from sequence☆25Updated 2 years ago
- Generate robust DNA barcode sets☆32Updated last year
- ☆38Updated last year
- Haplotype, isoform and gene level expression analysis using multi-mapping RNA-seq reads☆68Updated last year
- Absolute quantification package based on quantms.io☆15Updated 3 months ago
- predicts neoepitopes from phased somatic mutations detected using tumor/normal DNA-seq data☆27Updated last year
- A Computational Workflow for Designing Libraries of sgRNAs for CRISPR-Mediated Base Editing, and much more☆19Updated last year
- ✂️ Deep learning-based splice site predictor that improves spliced alignments☆54Updated 6 months ago
- Deep learning embedding for nucleotide sequences☆19Updated 5 months ago
- SPLICE-q -- A Python tool for genome-wide SPLIcing Efficiency quantification from RNA-seq data.☆12Updated last year
- Useful tools for working with Salmon output☆38Updated 5 years ago
- Ultra-fast 5' and 3' demultiplexer☆28Updated last year
- Identify and quantify MHC eluted peptides from mass spectrometry raw data☆38Updated 3 weeks ago
- Analyze antibody repertoires and discover new V genes from high-throughput sequencing reads☆16Updated last year
- ☆20Updated 3 months ago
- ☆18Updated last year