dewshr / NCBI-GenBank-file-parserLinks
This program can be used to parse the NCBI GenBank file to create a tabulated csv file.
☆10Updated 6 years ago
Alternatives and similar repositories for NCBI-GenBank-file-parser
Users that are interested in NCBI-GenBank-file-parser are comparing it to the libraries listed below
Sorting:
- A series of small Biopython scripts for downloading sequence data off NCBI's Genbank.☆15Updated 8 years ago
- Lecture on viral phylodynamics☆12Updated 3 years ago
- Chromatin ACcessibility and Transcriptomics Unifying Software☆17Updated 11 months ago
- PanGenomePipeline☆16Updated last year
- Python Programming for Biologists☆11Updated last month
- detection of duplications and deletions using Python based machine learning techniques☆28Updated 6 years ago
- ☆10Updated 13 years ago
- NASQAR: A web-based platform for High-throughput sequencing data analysis and visualization☆32Updated 5 years ago
- A command line tool to compute mapping statistics from a BAM file☆25Updated 3 years ago
- a Shiny/R application to view and annotate copy number variations☆28Updated 2 years ago
- FunctionaL Omics Processing platform☆13Updated last year
- A pipeline creation tool using Snakemake☆11Updated last week
- 🍶 Genome assembly with short sequence reads☆26Updated last year
- ChIP-seq pipeline tool for quality check, normalization, statistical analysis, and visualization of multiple ChIP-seq samples.☆24Updated 3 weeks ago
- ☆12Updated 6 years ago
- Analyze antibody repertoires and discover new V genes from high-throughput sequencing reads☆16Updated last year
- Rapid and accurate ancestry inference using SNVs.☆26Updated 2 months ago
- Method for performing genome-wide association like studies on neighborhoods identified on biological networks relevant for the phenotype …☆16Updated 2 years ago
- 🧬 MSABrowser: dynamic and fast visualization of sequence alignments, variations, and annotations☆35Updated last year
- Hybridization probe design for targeted genomic sequencing of diverse and hypervariable viral taxa☆25Updated 2 years ago
- We present a customizable computational tool, PathSeq2.0, to enable the discovery and identification of microbial sequences in metagenomi…☆11Updated 7 years ago
- ☆17Updated 3 years ago
- A very simple BLAST filtering pipeline☆18Updated 11 years ago
- Nanopore Real-Time Analysis Tool☆15Updated last year
- A Computational Workflow for Designing Libraries of sgRNAs for CRISPR-Mediated Base Editing, and much more☆19Updated last year
- SpliceWiz is an R package for exploring differential alternative splicing events in splice-aware alignment BAM files.☆21Updated 7 months ago
- Quality assessment of de novo transcriptome assemblies from RNA-Seq data☆25Updated 4 months ago
- A tool to extract LOH blocks from VCF, BAM and FASTA data☆25Updated last year
- CNV Rapid Aberration Detection And Reporting☆12Updated 4 years ago
- dv-trio provides a pipeline to call variants for a trio (father-mother-child) using DeepVariants [1]. Genomic Variant Calling Files (gVCF…☆11Updated 4 years ago