We present an open-source algorithm, Scalpel (http://scalpel.sourceforge.net/), which combines mapping and assembly for sensitive and specific discovery of insertions and deletions (indels) in exome-capture data. A detailed repeat analysis coupled with a self-tuning k-mer strategy allows Scalpel to outperform other state-of-the-art approaches for indel discovery, particularly in regions containing near-perfect repeats. We analyzed 593 families from the Simons Simplex Collection and demonstrated Scalpel's power to detect long (≥30 bp) transmitted events and enrichment for de novo likely gene-disrupting indels in autistic children
In this review, we focus on progress that has been made with detecting small insertions and deletion...
Small insertions and deletions (indels) are a common and functionally important type of sequence pol...
Motivation: While it was long assumed that most of the genomic variation within species is due to si...
As the second most common type of variation in the human genome, insertions and deletions (indels) h...
Insertion and deletion (INDEL) mutations, the most common type of structural variance, are associate...
<div><p>Insertion and deletion (INDEL) mutations, the most common type of structural variance, are a...
We report an algorithm to detect structural variation and indels from 1 base pair to 1 megabase pair...
Introduction: Indels (insertions/deletions) are important DNA sequence variations because of the hig...
Abstract Background Complex in...
Motivation: Insertions and deletions contribute significantly to genomic diversity both at intra and...
Abstract Background Insertions and deletions (indels) are a major class of genomic variation associa...
Motivation: There is a strong demand in the genomic community to develop effective algorithms to rel...
Repetitive sequences are abundant in the human genome. Different classes of repetitive DNA sequences...
Taking advantage of the deep targeted sequencing capabilities of next generation sequencers, we have...
A Publisher Correction to this article was published on 04 July 2018. This article has been updated....
In this review, we focus on progress that has been made with detecting small insertions and deletion...
Small insertions and deletions (indels) are a common and functionally important type of sequence pol...
Motivation: While it was long assumed that most of the genomic variation within species is due to si...
As the second most common type of variation in the human genome, insertions and deletions (indels) h...
Insertion and deletion (INDEL) mutations, the most common type of structural variance, are associate...
<div><p>Insertion and deletion (INDEL) mutations, the most common type of structural variance, are a...
We report an algorithm to detect structural variation and indels from 1 base pair to 1 megabase pair...
Introduction: Indels (insertions/deletions) are important DNA sequence variations because of the hig...
Abstract Background Complex in...
Motivation: Insertions and deletions contribute significantly to genomic diversity both at intra and...
Abstract Background Insertions and deletions (indels) are a major class of genomic variation associa...
Motivation: There is a strong demand in the genomic community to develop effective algorithms to rel...
Repetitive sequences are abundant in the human genome. Different classes of repetitive DNA sequences...
Taking advantage of the deep targeted sequencing capabilities of next generation sequencers, we have...
A Publisher Correction to this article was published on 04 July 2018. This article has been updated....
In this review, we focus on progress that has been made with detecting small insertions and deletion...
Small insertions and deletions (indels) are a common and functionally important type of sequence pol...
Motivation: While it was long assumed that most of the genomic variation within species is due to si...