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Osnat Ravid-Amir

dblp:16/8711 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2010
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 2 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › molecular evolution
mutation rate estimation
0.112010
Maximum likelihood estimation of locus-specific mutation rates in Y-chromosome short tandem repeats · Bioinform. 2010
Bioinformatics and computational biology
population genetics
0.112010
Maximum likelihood estimation of locus-specific mutation rates in Y-chromosome short tandem repeats · Bioinform. 2010

Methods — techniques the papers use, named apart from their topics

phylogenetic analysis · 0.1maximum likelihood estimation · 0.1
YearPublicationVenuePosition
2010 Maximum likelihood estimation of locus-specific mutation rates in Y-chromosome short tandem repeats
abstract
MOTIVATION: Y-chromosome short tandem repeats (Y-STRs) are widely used for population studies, forensic purposes and, potentially, the study of disease, therefore knowledge of their mutation rate is valuable. Here we show a novel method for estimation of site-specific Y-STR mutation rates from partial phylogenetic information, via the maximum likelihood framework. RESULTS: Given Y-STR data classified into haplogroups, we de-scribe the likelihood of observed data, and develop optimization strategies for deriving maximum likelihood estimates of mutation rates. We apply our method to Y-STR data from two recent papers. We show that our estimates are comparable, often more accurate than those obtained in familial studies, although our data sample is much smaller, and was not collected specifically for our study. Furthermore, we obtain mutation rate estimates for DYS388, DYS426, DYS457, three STRs for which there were no mutation rate measures until now.
Osnat Ravid-Amir, Saharon Rosset
Bioinform.1