Evidence map›Paper›PMID 19477993›Full record

ArticleBioinformatics (Oxford, England)2009

Joint estimation of gene conversion rates and mean conversion tract lengths from population SNP data.

Junming Yin, Michael I Jordan, Yun S Song

Open access · bronzeAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  3. A pedigree-based map of crossovers and non-crossovers in aye-ayes (bioRxiv : the preprint server for biology · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Junming YinComputer Science Division and Department of Statistics, University of California, Berkeley, CA, USA.
Michael I Jordan
Yun S Song
University of California, Berkeley · US

Funding

Protein function prediction by statistical phylogenomicsR01GM071749 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI BRENNER, STEVEN E · 2007 to 2010
$1.4M
Novel Methods for Characterizing Recombination and SelectionR00GM080099 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI SONG, YUN S · 2008 to 2010
$744k
NIGMS NIH HHS R00 GM080099NIGMS NIH HHS R00-GM080099NIGMS NIH HHS R01 GM071749NIGMS NIH HHS R01-GM071749
6 · The paper itself

Abstract

motivationTwo known types of meiotic recombination are crossovers and gene conversions. Although they leave behind different footprints in the genome, it is a challenging task to tease apart their relative contributions to the observed genetic variation. In particular, for a given population SNP dataset, the joint estimation of the crossover rate, the gene conversion rate and the mean conversion tract length is widely viewed as a very difficult problem.

resultsIn this article, we devise a likelihood-based method using an interleaved hidden Markov model (HMM) that can jointly estimate the aforementioned three parameters fundamental to recombination. Our method significantly improves upon a recently proposed method based on a factorial HMM. We show that modeling overlapping gene conversions is crucial for improving the joint estimation of the gene conversion rate and the mean conversion tract length. We test the performance of our method on simulated data. We then apply our method to analyze real biological data from the telomere of the X chromosome of Drosophila melanogaster, and show that the ratio of the gene conversion rate to the crossover rate for the region may not be nearly as high as previously claimed. AVAILABILITY: A software implementation of the algorithms discussed in this article is available at http://www.cs.berkeley.edu/ approximately yss/software.html.

Indexed as

AnimalsComputational BiologyCrossing Over, GeneticDrosophila melanogasterGene ConversionLikelihood FunctionsMarkov ChainsPolymorphism, Single NucleotideX Chromosome

Identifiers

PMID19477993
PMCPMC2687983
OpenAlexW2147757556

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.