Results for "Selective Sequencing"
Top-level pages
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...2698 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...2535 days ago
Awesome perl frameworks, libraries and software - PART 1
A curated list of awesome Perl frameworks, libraries and so...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...2502 days ago
Alignment-free sequence comparison tools available for next-generation sequencing data analysis
kallisto Transcript abundance quantification from RNA-seq data (uses p.../main/qcluster.html Reads error correction Lighter Correction of sequencing errors in raw, whole genome sequencing reads (k-mer based) Software...2384 days ago
Single Cell RNAseq data analysis tutorial !!
...rg/content/early/2016/09/02/036558 Citrus: A toolkit for single cell sequencing analysis http://biorxiv.org...amework for single-cell RNA-seq data https://github.com/PMBio/scLVM Selective Locally linear Inference of Ce...2363 days ago
- RNA-sequencing (RNA-seq) has a wide variety of applications, but no single analysis pipeline can be used in all cases. We review all of the major steps in RNA-seq data anal...
2363 days ago
PerlOneLiner for Bioinformatician
FILE SPACING------------ # Double space a fileperl -pe '$\="\n"'perl -pe 'BEGIN { $\="\n" }'perl -pe '$_ .= "\n"'pe...tes as hex numbers)perl -pi -e 's/\x89\xD8\x48\x8B/\x90\x90\x48\x8B/g' file SELECTIVE...2315 days ago
List of visualization tools for genome alignments
Genome browsers are useful not only for...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...2297 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...2287 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 analyze...Sciences, has over 11 years experience in molecular biology, next-generation sequencing based testing, clinical genom...2277 days ago
