Results for "LR"





Top-level pages

Wire posts

  • FastaQ 2 Fasta Oneliner: paste - - - -< totalRNA_placental_1.fastq | perl -pale'$_="@F[0..1]"'|tr "\^@" "\>" | perl -pale 's/\s/\n/g' #Oneliner #NGS #FastaQ #Fasta

    1302 days ago

  • Bioinformatics jobs #Evolution #EvolDir

    1225 days ago

  • +7 more Wire posts


  • Genomic Impact

    The ongoing genomic research in USA contributed $31 billion to the U.S. gross national product and helped support 152,000 jobs.  Reference:

    1619 days ago

  • New Vaccine Clears AIDS-Causing Virus in Monkeys

    ...& Science University’s Vaccine and Gene Therapy Institute. The new approach involves the use of cytomegalovirus, or CMV, a common virus already carried by a large percen...

    1550 days ago

  • +7 more News

Opportunity posts

ResearchLabs posts

  • LAPTI Lab

    ...understanding of how genetic information is decoded from DNA into RNA and proteins. Someone may find this topic a little strange and argue that we already know how this is happenin...

    1463 days ago





  • Pacbio Long Reads Compatible Software and Tools

    The following software packages are known to be compatible with PacBio® data, in addition to PacBio's own SMRT® Analysis suite. All packages are believed to be open source or freely available for non-commercial use. See the individual project sites for up-to-date license information. A se...

    Tags: Bioinformatics, Chromosome, Genome, NGS, Align, LongReads, LR, Reads, Pacbio

    274 days ago

  • Software and Tools to detect structure variation with long reads !!

    Uncovering the connection between genetics and heritable diseases requires an approach that looks at all the variant bases and types in a genome. While a PacBio de novo assembly resolves the most novel SV variants. 8-10X PacBio coverage of single genomes or trios reveals triple the SVs ...

    Tags: Bioinformatics, LR, Long, Reads, Tools, Software, Pacbio, Genome, DNA, Sequence, NGS, SV, Variation, Structure

    274 days ago