Genome Assembly Tools and Software - PART1 !!
...reads coverage information or sequencing reads. GAML 0.1 &n...pipeline for deep Illumina resequencing data. It assembles reads into..., like those produced by SMRT sequencing technologies (PacBio RS II) a...be used to characterize novel sequencing targets. SGA 0.10.14 &nd...2682 days ago
Quick next generation sequencing (NGS) terms definition
fragment size: the Illumina WGS protocol generates paired-end reads from both ends of longer fragments. The lengths of these fragments are assumed to be sampled from...2519 days ago
Awesome perl frameworks, libraries and software - PART 1
A curated list of awesome Perl frameworks, libraries an...n and collection of utilities for Next-Generation Sequencing (NGS) data analysis masukomi...bsp;- A Modern Perl Framework for High Throughput Sequencing analysis gbarr/perl-libnet&n...2486 days ago
Alignment-free sequence comparison tools available for next-generation sequencing data analysis
kallisto Transcript abundance quantification from RNA-seq data (use...n/main/qcluster.html Reads error correction Lighter Correction of sequencing errors in raw, whole genome sequencing reads (k-mer based) Software...2368 days ago
Single Cell RNAseq data analysis tutorial !!
A major breakthrough (replaced microarrays) in the late 00’s and has been w...iorxiv.org/content/early/2016/09/02/036558 Citrus: A toolkit for single cell sequencing analysis http://biorxiv.org/...2347 days ago
2347 days ago
List of visualization tools for genome alignments
Genome browsers are useful not only...sequence features, next-generation sequencing (NGS) data and the results of...of sequences derived from multiple sequencing technologies. Low- or high-de...que sequences in an entire Illumina sequencing run http://www.sourceforge.n...2280 days ago
Computational resources for TE discovery and TE detection
Transposable Elements (TEs) to genome structure and evolution as well as their impact on genome sequencing, assembly, annotation and ali...2271 days ago
Webinar on RNA-Seq Data Analysis on 28 Feb 2018
Strand NGS is a biologist friendly NGS analysis tool that allows biologists to anal...Sciences, has over 11 years experience in molecular biology, next-generation sequencing based testing, clinical genom...2261 days ago
Some useful Bioinformatics links
Reference-free prediction of rearrangeme...e European eel genome from nanopore sequencing reads | Scientific Reports h...t and sensitive mapping of nanopore sequencing reads with GraphMap | Nature...sembled de novo using only nanopore sequencing data | Nature Methods https:...2238 days ago