Evidence map›Paper›PMID 33995755›Full record

ArticleThe annals of applied statistics2020

SEQUENTIAL IMPORTANCE SAMPLING FOR MULTIRESOLUTION KINGMAN-TAJIMA COALESCENT COUNTING.

Lorenzo Cappello, Julia A Palacios

Abstract read
In one paragraph

Article in The annals of applied statistics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. An efficient coalescent model for heterochronously sampled molecular data.Journal of the American Statistical Association · 2024
    Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Lorenzo CappelloStanford University.
Julia A PalaciosStanford University.

Funding

Scalable Coalescent Inference for Large Data SetsR01GM131404 · NIGMS · STANFORD UNIVERSITY · PI PALACIOS, JULIA · 2018 to 2021
$1.2M
NIGMS NIH HHS R01 GM131404
6 · The paper itself

Abstract

Statistical inference of evolutionary parameters from molecular sequence data relies on coalescent models to account for the shared genealogical ancestry of the samples. However, inferential algorithms do not scale to available data sets. A strategy to improve computational efficiency is to rely on simpler coalescent and mutation models, resulting in smaller hidden state spaces. An estimate of the cardinality of the state-space of genealogical trees at different resolutions is essential to decide the best modeling strategy for a given dataset. To our knowledge, there is neither an exact nor approximate method to determine these cardinalities. We propose a sequential importance sampling algorithm to estimate the cardinality of the sample space of genealogical trees under different coalescent resolutions. Our sampling scheme proceeds sequentially across the set of combinatorial constraints imposed by the data, which in this work are completely linked sequences of DNA at a non recombining segment. We analyze the cardinality of different genealogical tree spaces on simulations to study the settings that favor coarser resolutions. We apply our method to estimate the cardinality of genealogical tree spaces from mtDNA data from the 1000 genomes and a sample from a Melanesian population at the

Indexed as

coalescentenumerationsequential importance sampling

Identifiers

PMID33995755
PMCPMC8118586

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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.