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• • Jitendra Narayan@admin

  

  Reference-free Prediction of Rearrangement Breakpoint Reads http://bioinformatics.oxfordjournals.org/content/early/2014/05/28/bioinformatics.btu360.short #Reference #Breakpoint #Reads #Rearrangement

  3518 days ago

• • Jitendra Narayan@admin

  

  A survey of tools for variant analysis of next-generation genome sequencing data http://bib.oxfordjournals.org/content/15/2/256.short #NGS #Tools #Survey #Variant

  3518 days ago

• • Robert M Willioms@robert

  

  A tool set for short variant discovery in genetic sequence data. http://genome.sph.umich.edu/wiki/Vt #Tool #VT #Variant

  3518 days ago

• • Jitendra Narayan@admin

  

  MICC package for chromatin interaction http://bioinformatics.oxfordjournals.org/content/early/2015/07/31/bioinformatics.btv445.short #R #Chromatin #Package #Interaction #ChIA-PET

  3171 days ago

• • Rahul Agarwal@raag

  

  Nice Short Review-Disease Biomarkers for Precision Medicine: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414969/ #Omics #Cancer #PrecisionMedice

  2311 days ago

• • Jit@jit.aber

  

  #Short #read #alignment: an #introduction https://www.sevenbridges.com/short-read-alignment-algorithms/

  2172 days ago

• • Jit@jit.aber

  

  I recommend two technologies: long reads to get the genome right, short reads to get the bases right. #Genome #Assembly #Reads #LonfReads

  1942 days ago

• • Abhimanyu Singh@abhimanyu

  

  long #Pacbio sequence reads to #assemble a #bacterial genome, including correcting the assembly with short Illumina reads. http://sepsis-omics.github.io/tutorials/modules/cmdline_assembly/

  1852 days ago

• • Jit@jit.aber

  

  #Improving draft #assemblies by iterative mapping and #assembly of short reads to eliminate #gaps https://genomebiology.biomedcentral.com/articles/10.1186/gb-2010-11-4-r41

  1552 days ago

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