finkelsteinlab / freebarcodesLinks
FREE Divergence Error-Correcting DNA Barcodes
☆9Updated 7 years ago
Alternatives and similar repositories for freebarcodes
Users that are interested in freebarcodes are comparing it to the libraries listed below
Sorting:
- interactive plots for differential expression analysis☆32Updated last week
- A program for fast and accurate genome-guided transcripts reconstruction and quantification from RNA-seq (Supporting Pacbio single-end)☆23Updated 4 years ago
- ☆21Updated last year
- ☆20Updated last month
- The R package "sarlacc" contains a pipeline to analyse nanopore sequencing data. It trims adapter sequences, retrieves optional UMI's, cl…☆13Updated 6 years ago
- Relative Abundance of Transcripts: An R package for the detection of Differential Transcript isoform Usage.☆34Updated 3 years ago
- Chromatin segmentation in R☆19Updated 7 years ago
- R Interface to the NCBI SRA metadata☆23Updated 6 years ago
- Summarize and filter read alignments from multiple sequencing samples (taken as sorted BAM files)☆17Updated 2 weeks ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 3 years ago
- ☆14Updated 2 years ago
- ☆16Updated last year
- AnaLysis routines for ePigenomicS data - 🏫 Bioconductor project☆16Updated last year
- Useful tools for working with Salmon output☆38Updated 5 years ago
- 📊 An R package of RNA-seq workflow☆16Updated 3 years ago
- curPrimers is a tool for trimming primer sequences from amplicon based NGS reads☆16Updated last month
- a Shiny/R application to view and annotate copy number variations☆28Updated 2 years ago
- Calib clusters barcode tagged paired-end reads based on their barcode and sequence similarity.☆38Updated 2 years ago
- ☆22Updated last week
- Supplementary information to "Computational correction of index switching in multiplexed sequencing libraries" (Larsson et. al 2018).☆15Updated 4 years ago
- End-guided RNA assembler☆15Updated 2 months ago
- methylR: a single shiny solution from sequencer data to pathway analysis☆12Updated 7 months ago
- Comprehensive Human Expressed SequenceS☆17Updated 10 months ago
- A small R package to make sequencing read coverage plots in R.☆38Updated 3 years ago
- A command line tool to compute mapping statistics from a BAM file☆24Updated 3 years ago
- Rapid and accurate ancestry inference using SNVs.☆19Updated 2 weeks ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year
- TIMEOR: Trajectory Inference and Mechanism Exploration with Omics Data in R☆17Updated 3 years ago
- Exhaustive capture of biological variation in RNA-seq data through k-mer decomposition.☆15Updated 6 years ago
- ☆28Updated 6 months ago