BOL

Results for "sequencing"

Tags

• • pradyumna Jayaram@pradyumnasagar

  

  Comparison of mapping tools !

  There are many mapping tools, and each one has its own specifications. Once we have two or more tools for similar purposes, how can we say which tool is better?

  Tags: NGS, Mapping, Sequencing

  2957 days ago

• • Radha Agarkar@radhaagarkar

  

  cutadapt

  Cutadapt finds and removes adapter sequences, primers, poly-A tails and other types of unwanted sequence from your high-throughput sequencing reads. Cleaning your data in this way is often required: Reads from small-RNA sequencing contain the 3’ sequencing adapter because the read is longe...

  Tags: Bioinformatics, Cutadapt, NGS, Reads, Fastq, Sequencing

  2904 days ago

• • Jit@jit.aber

  

  Coming of age: ten years of next-generation sequencing technologies http://www.nature.com/nrg/journal/v17/n6/full/nrg.2016.49.html #Sequencing #Technology #NGS #Updates

  Tags: Sequencing, Technology, NGS, Updates

  2894 days ago

• • Jit@jit.aber

  

  LoRMA: a tool for correcting sequencing errors in long reads such those produced by Pacific Biosciences sequencing machines

  LoRMA is a tool for correcting sequencing errors in long reads such those produced by Pacific Biosciences sequencing machines. Publication: L. Salmela, R. Walve, E. Rivals, and E. Ukkonen: Accurate selfcorrection of errors in long reads using de Bruijn graphs. Accepted to RECOMB-Seq 2016. ...

  Tags: Bioinformatics, LoRMA, Tool, Correcting, Errors, Reads, Sequencing

  2155 days ago

• • Jit@jit.aber

  

  CovCal: Coverage / Read Count Calculator

  Coverage / Read Count Calculator Calculate how much sequencing you need to hit a target depth of coverage (or vice versa). Instructions: set the read length/configuration and genome size, then select what you want to calculate. Written by Stephen Turner, based on the Lander-Waterman formula, i...

  Tags: Bioinformatics, covcal, Tool, Coverage, Reads, Sequencing

  2155 days ago

• • Neelam Jha@neelam

  

  #Training in High-Throughput #Sequencing: Common #Guidelines to Enable #Material Sharing, Dissemination, and Reusability http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1004937

  Tags: Training, Sequencing, Guidelines, Material

  2868 days ago

• • Abhimanyu Singh@abhimanyu

  

  #Duplication #FastQC http://proteo.me.uk/2013/09/a-new-way-to-look-at-duplication-in-fastqc-v0-11/ #Sequencing #NGS

  Tags: Duplication, FastQC, Sequencing, NGS

  2834 days ago

• • Shruti Paniwala@shruti

  

  Long-read human genome sequencing and its applications https://www.nature.com/articles/s41576-020-0236-x #LongReads #Sequencing #Genome #Review

  Tags: LongReads, Sequencing, Genome, Review

  1416 days ago

• • Strand@Strand

  

  Live Webinar on RNA-Seq Data Analysis on 9 Nov 2016

  Live Webinar on RNA-Seq Data Analysis Abstract: Strand NGS supports an extensive workflow for the analysis and visualization of RNA-Seq data. The workflow includes Transcriptome / Genome alignment, Differential expression analysis with Statistical approach and Splicing events detection. Strand N...

  Tags: Strand NGS, Webinar, RNA-Seq, NGS, Sequencing

  2745 days ago

• • Jit@jit.aber

  

  GAM-NGS: genomic assemblies merger for next generation sequencing

  GAM-NGS is a tool able to merge two or more assemblies in order to improve contiguity and correctness. It can be used on all NGS-based assembly projects and it shows its full potential with multi-library Illumina-based projects. With more than 20 available assemblers it is hard to select the best...

  Tags: GAM-NGS, Genomic, Assemblies, Merger, Sequencing, NGS

  2533 days ago

• « Previous
• 1
• 2
• 3
• 4
• 5
• 6
• 7
• 8
• 9
• 10
• Next »