AGE: defining breakpoints of genomic structural variants at single-nucleotide resolution, through optimal alignments with gap excision

Lignende værker

• LongAGE: defining breakpoints of genomic structural variants through optimal and memory efficient alignments of long reads
  af: Tran, Quang, et al.
  Udgivet: (2020)
• Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library
  af: Lam, Hugo Y. K., et al.
  Udgivet: (2009)
• Elevated variant density around SV breakpoints in germline lineage lends support to error-prone replication hypothesis
  af: Dhokarh, Dhananjay, et al.
  Udgivet: (2016)
• Single-nucleotide resolution analysis of nucleotide excision repair of ribosomal DNA in humans and mice
  af: Yang, Yanyan, et al.
  Udgivet: (2019)
• MAP: Mutation Arranger for Defining Phenotype-Related Single-Nucleotide Variant
  af: Baek, In-Pyo, et al.
  Udgivet: (2014)