Evidence map›Paper›PMID 35647675›Full record

ArticleMolecular biology and evolution2022

distAngsd: Fast and Accurate Inference of Genetic Distances for Next-Generation Sequencing Data.

Lei Zhao, Rasmus Nielsen, Thorfinn Sand Korneliussen

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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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.

Lei ZhaoSection for Geogenetics, Globe Institute, University of Copenhagen, Øster Voldgade 5-7, 1350 København K, Denmark.ORCID 0000-0002-6551-2707
Rasmus NielsenSection for Geogenetics, Globe Institute, University of Copenhagen, Øster Voldgade 5-7, 1350 København K, Denmark.ORCID 0000-0003-0513-6591
Thorfinn Sand KorneliussenSection for Geogenetics, Globe Institute, University of Copenhagen, Øster Voldgade 5-7, 1350 København K, Denmark.ORCID 0000-0001-7576-5380

Funding

Enabling Precision Genomics Using Adaptive VariationR01GM138634 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI NIELSEN, RASMUS · 2020 to 2023
$1.7M
NIGMS NIH HHS R01 GM138634
6 · The paper itself

Abstract

Commonly used methods for inferring phylogenies were designed before the emergence of high-throughput sequencing and can generally not accommodate the challenges associated with noisy, diploid sequencing data. In many applications, diploid genomes are still treated as haploid through the use of ambiguity characters; while the uncertainty in genotype calling-arising as a consequence of the sequencing technology-is ignored. In order to address this problem, we describe two new probabilistic approaches for estimating genetic distances: distAngsd-geno and distAngsd-nuc, both implemented in a software suite named distAngsd. These methods are specifically designed for next-generation sequencing data, utilize the full information from the data, and take uncertainty in genotype calling into account. Through extensive simulations, we show that these new methods are markedly more accurate and have more stable statistical behaviors than other currently available methods for estimating genetic distances-even for very low depth data with high error rates.

Indexed as

GenomeHigh-Throughput Nucleotide SequencingAlgorithmsDiploidyGenotypePolymorphism, Single NucleotideSequence Analysis, DNASoftwareexpectation maximizationgenetic distancegenotype likelihoodhigh-throughput sequencingmaximum likelihoodmolecular evolutionnext-generation sequencingphylogeny reconstruction

Identifiers

PMID35647675
PMCPMC9234764

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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.