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Results for "DNA-seq"

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• • LEGE@lege

  

  Comment on "Tools for Sequence translation !"

  Sequence translation is the process of converting a DNA or RNA sequence into its corresponding protein sequence. This is an important step in the an...

  420 days ago

• • Rahul Agarwal@raag

  

  Comment on "China’s BGI says it can sequence a genome for just $100"

  https://www.bloomberg.com/news/features/2019-11-13/chinese-genetics-giant-bgi-wants-to-tailor-medicine-to-your-dna

  1526 days ago

• • Rahul Agarwal@raag

  

  Comment on "China’s BGI says it can sequence a genome for just $100"

  https://news.bloomberglaw.com/ip-law/illumina-hits-rival-bgi-with-new-dna-sequencing-patent-lawsuit

  1526 days ago

• • Rahul Nayak@rahul

  

  Comment on "Tools for Searching Repeats And Palindromic Sequences"

  Check out this GAP-Seq: a method for identification of DNA palindromes https://bmcgenomics.biomedcentral.com/articles/10.1186/1471-2164-15-394

  1534 days ago

• • Neelam Jha@neelam

  

  Comment on "Learn Genetics Online"

  This is one of the best interative genomics tutorial that I found useful. Have a look https://lab.concord.org/embeddable.html#interactives/sam/DNA-to-proteins/1-dna-to-protein.json

  1557 days ago

• • Jit@jit.aber

  

  Comment on "List of motif discovery tools !"

  Motif algorithms  This link on Nature explain: how does DNA sequence motif discovery work? Paper on BMC bioinformatics: survey of DNA motif finding algorithms This paper discusses some limitations and potentials of motif discovery algorithms (2005)

  1981 days ago

• • Jit@jit.aber

  

  Comment on "AfterQC: Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data"

  AfterQC AfterQC - Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data. dupRadar dupRadar. An R package which provide...

  2136 days ago

• • Rahul Nayak@rahul

  

  Comment on "Bioinformatics tools developed for Oxford Nanopore data analysis !"

  NanoComp: comparing multiple runs NanoStat: statistic summary report of reads or alignments NanoFilt: filtering and trimming of reads NanoLyse: removing contaminant reads (e.g. lambda control DNA) from fastq

  2252 days ago

• • Jit@jit.aber

  

  Comment on "Important Journals, Blogs and Forums for Bioinformaticians"

  Informative bioinformatics bloggers Diving into Genetics and Genomics YOKOFAKUN  Getting Genetics Done Gigabase or gigabyte Genome Spot  CoreGenomics T...

  2319 days ago

• • Jit@jit.aber

  

  Comment on "List of bioinformatics companies and genomics service providers"

  Inside DNA, Computing platform for reproducible research in bioinformatics, genomics and life science https://insidedna.me/

  2626 days ago

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