ArticleBioinformatics (Oxford, England)2012
Blockwise HMM computation for large-scale population genomic inference.
Article in Bioinformatics (Oxford, England), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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.
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.
Who cites it
11 citing papers in PubMed.
- Robust and accurate Bayesian inference of genome-wide genealogies for hundreds of genomes.Nature genetics · 2025Article
- Article
- Scaling the Discrete-time Wright Fisher model to biobank-scale datasets.bioRxiv : the preprint server for biology · 2023Article
- Privacy-preserving genotype imputation in a trusted execution environment.Cell systems · 2021Article
- Genetic adaptation of Tibetan poplar (Ecology and evolution · 2020Article
- Inference of complex population histories using whole-genome sequences from multiple populations.Proceedings of the National Academy of Sciences of the United States of America · 2019Article
- Inference of population history using coalescent HMMs: review and outlook.Current opinion in genetics & development · 2018Review
- Robust and scalable inference of population history from hundreds of unphased whole genomes.Nature genetics · 2017Article
- Next-generation genotype imputation service and methods.Nature genetics · 2016Article
- A sequentially Markov conditional sampling distribution for structured populations with migration and recombination.Theoretical population biology · 2013Article
- Estimating variable effective population sizes from multiple genomes: a sequentially markov conditional sampling distribution approach.Genetics · 2013Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
motivationA promising class of methods for large-scale population genomic inference use the conditional sampling distribution (CSD), which approximates the probability of sampling an individual with a particular DNA sequence, given that a collection of sequences from the population has already been observed. The CSD has a wide range of applications, including imputing missing sequence data, estimating recombination rates, inferring human colonization history and identifying tracts of distinct ancestry in admixed populations. Most well-used CSDs are based on hidden Markov models (HMMs). Although computationally efficient in principle, methods resulting from the common implementation of the relevant HMM techniques remain intractable for large genomic datasets.
resultsTo address this issue, a set of algorithmic improvements for performing the exact HMM computation is introduced here, by exploiting the particular structure of the CSD and typical characteristics of genomic data. It is empirically demonstrated that these improvements result in a speedup of several orders of magnitude for large datasets and that the speedup continues to increase with the number of sequences. The optimized algorithms can be adopted in methods for various applications, including the ones mentioned above and make previously impracticable analyses possible. AVAILABILITY: Software available upon request. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. CONTACT: yss@eecs.berkeley.edu.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.