Results for "Deletions"


  • DiscoSnp

    DiscoSnp is designed for discovering all kinds of SNPs (not only isolated ones), as well as insertions and deletions, from raw set(s) of reads. The number of input read sets is not constrained, it can be one, two, or more. No reference genome is needed.

    89 days ago

  • DIAL

    ...ce genome. DIAL works even when the depth of coverage is insufficient for de novo assembly, and it can be extended to determine small insertions/deletions. Our main motivation is to us...

    353 days ago

  • Stampy

    ...s in the mapping of reads containing that contain sequence variation relative to the reference, in particular for those containing insertions or deletions.

    638 days ago

  • GenomeComp

    ...zing the genome wide sequence comparison results derived from voluminous BLAST textual output, so as to locate the rearrangements, insertions or deletions of genome segments between sp...

    365 days ago

  • ACANA: An accurate and consistent alignment tool for DNA sequences

    ...pecifically designed for aligning sequences that share only some moderately conserved regions and/or have a high frequency of long insertions or deletions. It attempts to combine the b...

    73 days ago

  • segemehl map short sequencer reads to reference genomes. Unlike other methods, segemehl is able to detect not only mismatches but also insertions and deletions. Furthermore, segemehl is not...

    648 days ago

  • MGRA: Breakpoint graphs and ancestral genome reconstructions

    ...e MGRA can reconstruct conserved ancestral regions (CARs) of the ancestral genome of interest. Since version 2 MGRA supports gene insertion and deletions in addition to genome rearran...

    207 days ago

  • GenomeRing: alignment visualization based on SuperGenome coordinates

    ...yses of genomic variation. Such analyses are often based on whole-genome alignments to elucidate structural differences arising from insertions, deletions or from rearrangement events....

    395 days ago


    ...n across a structrual variant -- SV ) mapping and SV calling from the mapping result. PRISM is able to detect small insertions and abitrary size deletions, inversions and tandom duplic...

    434 days ago

  • MOSAIK: A Hash-Based Algorithm for Accurate Next-Generation Sequencing Short-Read Mapping

    ...clustering strategy coupled with the Smith-Waterman algorithm. This method is well-suited to capture mismatches as well as short insertions and deletions. To support the growing inter...

    638 days ago