indel


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indel

(ĭn′dĕl′)
n.
A genetic mutation caused by the insertion or deletion of a segment of DNA into an organism's genome.

indel

(in′del″) [ in(sertion) + del(etion)]
Insertions in and deletions from strands of DNA.
References in periodicals archive ?
Predicting the functional effect of amino acid substitutions and indels.
As for FSHb, an indel was found to be significantly associated with testis long circumference (TLC) (P = 0.
Most noticeably, the Nageswari duck population had the largest number of unique haplotypes (Hap_10 to Hap_20) and a specific indel, suggesting it is a distinct variety of indigenous Bangladeshi duck.
At each position, we defined the major allele count as the highest nucleotide count, the minor allele count as the second highest nucleotide count, the SNV background count as depth minus the major count, and the INDEL background count as the sum of insertion and deletion counts.
They differ from each other by a single 14 bp indel, and from the others by two indels, six transversions and 2 transitions.
This study investigated the relationship between ACE indel polymorphisms and cardiorespiratory fitness in a sample of both physically active and sedentary Caucasian women from Brazil.
The addition of the five sequences and the reduction in the number of taxa resulted in an alignment adjustment with a consequent change in the trnL indel presence/absence matrix.
Also, most of the extensive INDEL variation (insertion/deletion mutations) between chimps and humans (26,509 sites) is due to Alu insertions in the human lineage, insertions which correlate with significant differences in gene expression and with large INDEL variation close to coding loci.
Located within Renarte's corporate office premises, it offers clients a view of the company's product catalogue across various brands such as Paderno, Indel, Dudson, Royal Bone China and Guy Degrenne among others.
The C8[alpha] MACPF sequence is distinctive in that it contains a unique indel (insertion/deletion) between residues 159-175, which includes C164 that forms the disulfide bond to C40 in C8[gamma].
Se identificaron polimorfismos de tipo SNPs e indel en tres variedades de yuca en una region parcial del gen candidato de resistencia RXam2.