ChillarAnand / fadapaLinks
FAstqc DAta PArser - A minimal parser to parse FastQC output data.
☆16Updated 9 years ago
Alternatives and similar repositories for fadapa
Users that are interested in fadapa are comparing it to the libraries listed below
Sorting:
- reference free variant assembly☆33Updated last year
- ☆19Updated 8 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 5 months ago
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Updated 7 years ago
- ☆37Updated 4 years ago
- blast, shmlast☆22Updated 4 years ago
- Ococo: the first online variant and consensus caller. Call genomic consensus directly from an unsorted SAM/BAM stream.☆47Updated 6 years ago
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 5 years ago
- Stupid Simple Structural Variant View☆25Updated 8 years ago
- Using reference-free compressed data structures to analyse thousands of human genomes (1000 Genomes ReadServer)☆14Updated 7 years ago
- FAST: Fast Analysis of Sequences Toolbox☆31Updated 5 years ago
- ☆26Updated 4 years ago
- Pipeline for poreathon☆14Updated 10 years ago
- Rapid competitive read demulitplexer. Made with tries.☆23Updated 2 weeks ago
- Integrated Variant Caller☆17Updated 7 years ago
- Metagenomic profiling and phylogenetic distances via common kmers☆42Updated 3 years ago
- Course material for the de novo assembly part of the INF-BIO9120 course at Univ. of Oslo Fall 2013☆37Updated 11 years ago
- full taxonomer cython repository☆22Updated 5 years ago
- DNA assembler developed on FER (Croatia), RBI (Croatia) and GIS (Singapore)☆18Updated 9 years ago
- robust matching of small variant datasets using flexible scoring schemes☆10Updated 5 years ago
- Novel Adjacency Identification with Barcoded Reads☆13Updated 3 years ago
- BigWig manpulation tools using libBigWig and htslib☆29Updated 9 months ago
- Malleable All-seeing Journal Of Research Artifacts☆36Updated 2 years ago
- Color DNA/RNA bases in terminal output☆21Updated 7 years ago
- Visualise interstrain recombination from environmental samples.☆26Updated 6 years ago
- Ximmer is a system for CNV calling on exome and targeted genomic sequencing☆19Updated 3 months ago
- variant discovery and annotation using GATK and Ensembl☆17Updated 11 years ago
- Sample an approximate number of reads from a fastq file without reading the entire file☆11Updated 7 years ago
- An ultra fast and accurate paired-end adapter trimmer that needs no a priori adapter sequences.☆22Updated 4 years ago
- Mapping-free variant caller for short-read Illumina data☆19Updated 5 years ago