Evidence map›Paper›PMID 37147657›Full record

ArticleAlgorithms for molecular biology : AMB2023

Pangenomic genotyping with the marker array.

Taher Mun, Naga Sai Kavya Vaddadi, Ben Langmead

Abstract read
In one paragraph

Article in Algorithms for molecular biology : AMB, 2023. 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

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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Integer programming framework for pangenome-based genome inference.bioRxiv : the preprint server for biology · 2024
    Article
  5. Review
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.

Taher MunDepartment of Computer Science, Johns Hopkins University, Baltimore, MD, USA.
Naga Sai Kavya VaddadiDepartment of Computer Science, Johns Hopkins University, Baltimore, MD, USA.
Ben LangmeadDepartment of Computer Science, Johns Hopkins University, Baltimore, MD, USA. langmea@cs.jhu.edu.

Funding

Methods for sequencing data analysis and archive-scale data science - RenewalR35GM139602 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Benjamin Thomas Langmead · 2021 to 2026
$5.0M
Personal and panel references for improved alignmentR01HG011392 · NHGRI · JOHNS HOPKINS UNIVERSITY · PI LANGMEAD, BENJAMIN THOMAS · 2020 to 2025
$4.2M
NHGRI NIH HHS R01 HG011392NHGRI NIH HHS R01HG011392NIGMS NIH HHS R35 GM139602NIGMS NIH HHS R35GM139602
6 · The paper itself

Abstract

We present a new method and software tool called rowbowt that applies a pangenome index to the problem of inferring genotypes from short-read sequencing data. The method uses a novel indexing structure called the marker array. Using the marker array, we can genotype variants with respect from large panels like the 1000 Genomes Project while reducing the reference bias that results when aligning to a single linear reference. rowbowt can infer accurate genotypes in less time and memory compared to existing graph-based methods. The method is implemented in the open source software tool rowbowt available at https://github.com/alshai/rowbowt .

Indexed as

GenotypingIndexingSequence alignment

Identifiers

PMID37147657
PMCPMC10161648

What OpenQuestion holds

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Registered trials

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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.