Evidence map›Paper›PMID 37388907›Full record

ArticleCell genomics2023

The landscape of somatic mutations in lymphoblastoid cell lines.

Madison Caballero, Amnon Koren

Erratum issuedAbstract read
In one paragraph

Article in Cell genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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. A sibling study of variation in parental mutation rates.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Madison CaballeroDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA.
Amnon KorenDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA.

Funding

Personal mutational landscapes encoded in our DNADP2GM123495 · NIGMS · CORNELL UNIVERSITY · PI KOREN, AMNON · 2016 to 2016
$2.3M
NIGMS NIH HHS DP2 GM123495
6 · The paper itself

Abstract

Somatic mutations have important biological ramifications while exerting substantial rate, type, and genomic location heterogeneity. Yet, their sporadic occurrence makes them difficult to study at scale and across individuals. Lymphoblastoid cell lines (LCLs), a model system for human population and functional genomics, harbor large numbers of somatic mutations and have been extensively genotyped. By comparing 1,662 LCLs, we report that the mutational landscape of the genome varies across individuals in terms of the number of mutations, their genomic locations, and their spectra; this variation may itself be modulated by somatic

Indexed as

chronic lymphocytic leukemialymphoblastoid cell linesmutational signaturesmutationsreplication timing

Identifiers

PMID37388907
PMCPMC10300552

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.