indels

The 1.5 – 2% difference between humans and chimps is still a valid number so long as you point out what it's in reference to (alignable nucleotides, ignoring indels).

A Dubious "Opportunity" for IDers 2007

The 1.5 – 2% difference between humans and chimps is still a valid number so long as you point out what it's in reference to (alignable nucleotides, ignoring indels).

A Dubious "Opportunity" for IDers 2007

Collectively insertions and deletions are known as “indels”.

Logarithmic Gap Costs Decrease Alignment Accuracy - The Panda's Thumb 2007

Only with indels insertions/deletions and similar events where a single mutation removes or copies many base pairs at once, do you get the larger numbers.

A new (mis)take on an old paper - The Panda's Thumb 2007

Remember that the “125 bases” includes not only point mutations, but indels which counts as multiples.

How fast can evolution work? - The Panda's Thumb 2007

Collectively insertions and deletions are known as “indels”.

The Panda's Thumb: January 2007 Archives 2007

Abstract: Recent studies show that along with single nucleotide polymorphisms and small indels, larger structural differences contribute significantly to human genetic diversity.

Information Technology at Indiana University: News In Focus 2010

A variant ascertainment algorithm that can be used to detect SNPs, indels, and other polymorphisms

Gentoo Packages Unknown ( 2010

(SNPs) and three indels, including a 33 kbp prophage that accounted for the observed difference in AscI PFGE patterns.

BioMed Central - Latest articles 2010

In particular, the study of point mutations (here used in the sense that includes relatively small insertions and deletions, or indels) on genes has led to deep understandings of many aspects of genome evolution

PLoS ONE Alerts: New Articles Hong-Da Chen et al. 2010

Researchers can assemble these fragments into ‘contigs’ that reveal relatively small differences such as single-nucleotide variants and ‘indels’ — insertions or deletions of a handful of nucleotides — but that cannot resolve larger structural variations.

Every base everywhere all at once: pangenomics comes of age Michael Eisenstein 2023

Researchers can assemble these fragments into ‘contigs’ that reveal relatively small differences such as single-nucleotide variants and ‘indels’ — insertions or deletions of a handful of nucleotides — but that cannot resolve larger structural variations.

Every base everywhere all at once: pangenomics comes of age Michael Eisenstein 2023