read data generator

Convert NGS reads to analysis ready variants with GATK's ReadsPipelineSpark

Genome read alignments visualizer

Preprocessing of raw reads obtained using ARTIC's protocol for sequencing SARS-CoV-2 genome.

GPSeq sequencing data analysis pipeline

Software for cleaning fastq reads with or without adapter list

Complete Pipeline for RNA-seq data analysis: From FastQ to differntial gene expression to annotated Variations.

This library content most interesting reads for any mobile developer and another. All book's will be added our member's for you!

Python code to detect ECGR Mutations; Takes a reference genome and bunch of reads as input and finds mutations (1-3 bp length) where number of supporting reads greater than 5

A Guide to Automatically Downloading NCBI SRA Reads

hierarchical clustering of DNA sequence using upcxx

Filter alignments on sequence length and/or identity of first nucleotide.

Temperature, Relative Humidity, Atmospheric Pressure Logger program, displays and saves data to a csv file

a simple in-memory key-value (KV) store as a client-server application running over TCP sockets,

Heterozygous aware long reads corrector !

📚 A list of physical books I own or want to read.

R functions and workflow for submitting amplicon sequence data to the ENA.

Study material (pdfs, notes, free course download links etc) for HACKERS

Sanyojan is a highly sensitive, hybrid genome assembler.