Evidence map›Paper›PMID 30669964›Full record

ArticleBMC bioinformatics2019

s-dePooler: determination of polymorphism carriers from overlapping DNA pools.

Aleksandr Igorevich Zhernakov, Alexey Mikhailovich Afonin, Natalia Dmitrievna Gavriliuk, Olga Mikhailovna Moiseeva, Vladimir Aleksandrovich Zhukov

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Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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2 citing papers in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Aleksandr Igorevich ZhernakovResearch Department of Non-Coronary Heart Diseases, Almazov National Medical Research Center, Ministry of Health of Russia, 2 Akkuratova St., St. Petersburg, 197341, Russia. AZhernakov@arriam.ru.ORCID http://orcid.org/0000-0001-8961-9317
Alexey Mikhailovich AfoninAll-Russia Research Institute for Agricultural Microbiology (ARRIAM), 3 Podbelsky Ch., St. Petersburg - Pushkin, 196608, Russia.
Natalia Dmitrievna GavriliukResearch Department of Non-Coronary Heart Diseases, Almazov National Medical Research Center, Ministry of Health of Russia, 2 Akkuratova St., St. Petersburg, 197341, Russia.
Olga Mikhailovna MoiseevaResearch Department of Non-Coronary Heart Diseases, Almazov National Medical Research Center, Ministry of Health of Russia, 2 Akkuratova St., St. Petersburg, 197341, Russia.
Vladimir Aleksandrovich ZhukovResearch Department of Non-Coronary Heart Diseases, Almazov National Medical Research Center, Ministry of Health of Russia, 2 Akkuratova St., St. Petersburg, 197341, Russia.

Funding

Russian Science Support Foundation 17-75-30052
6 · The paper itself

Abstract

backgroundSamples pooling is a method widely used in studies to reduce costs and labour. DNA sample pooling combined with massive parallel sequencing is a powerful tool for discovering DNA variants (polymorphisms) in large analysing populations, which is the base of such research fields as Genome-Wide Association Studies, evolutionary and population studies, etc. Usage of overlapping pools where each sample is present in multiple pools can enhance the accuracy of polymorphism detection and allow identifying carriers of rare-variants. Surprisingly there is a lack of tools for result interpretation and carrier identification, i.e. for "depooling".

resultsHere we present s-dePooler, the application for analysis of pooling experiments data. s-dePooler uses the variants information (VCF-file) and the pooling scheme to produce a list of candidate carriers for each polymorphism. We incorporated s-dePooler into a pipeline (dePoP) for automation of pooling analysis. The performance of the pipeline was tested on a synthetic dataset built using the 1000 Genomes Project data, resulting in the successful identification 97% of carriers of polymorphisms present in fewer than ~ 10% of carriers.

conclusionss-dePooler along with dePoP can be used to identify carriers of polymorphisms in overlapping pools, and is compatible with any pooling scheme with equivalent molar ratios of pooled samples. s-dePooler and dePoP with usage instructions and test data are freely available at https://github.com/lab9arriam/depop .

Indexed as

DNAGenome-Wide Association StudyHumansPolymorphism, GeneticSequence Analysis, DNADNADepoolingDNA poolsOverlapping poolsPolymorphism discoverySample pooling

Identifiers

PMID30669964
PMCPMC6343301

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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.