Evidence map›Paper›PMID 41040405›Full record

ArticlebioRxiv : the preprint server for biology2025

simPIC:flexible simulation of paired-insertion counts for single-cell ATAC sequencing data.

Sagrika Chugh, Heejung Shim, Davis J McCarthy

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Sagrika ChughBioinformatics and Cellular Genomics, St. Vincent's Institute of Medical Research, 9 Princes Street, Fitzroy, 3065, Victoria, Australia.ORCID 0000-0002-8050-5214
Heejung ShimSchool of Mathematics and Statistics, Faculty of Science, University of Melbourne, Grattan Street, Parkville, 3010, Victoria, Australia.ORCID 0000-0002-1375-9310
Davis J McCarthyBioinformatics and Cellular Genomics, St. Vincent's Institute of Medical Research, 9 Princes Street, Fitzroy, 3065, Victoria, Australia.ORCID 0000-0002-2218-6833

Funding

Integrated analysis of multi-omic QTLs at single cell resolutionR01HG011886 · NHGRI · TRANSLATIONAL GENOMICS RESEARCH INST · PI BANOVICH, NICHOLAS ELI · 2022 to 2025
$2.9M
NHGRI NIH HHS R01 HG011886
6 · The paper itself

Abstract

Single-cell Assay for Transposase Accessible Chromatin (scATAC-seq) is increasingly used at population scale to study how genetic variation shapes chromatin accessibility across diverse cell types. This widespread adoption of the assay has created a need for computational methods that can handle complex biological and technical variation. Yet method development is limited by the lack of flexible simulation tools with known ground truth. Here, we present simPIC, a simulation framework for generating realistic single-cell ATAC-seq data across individuals and cell types. simPIC supports both population-scale and single-individual simulations, with the ability to model cell groups, batch effects, and genotype-dependent variation in accessibility. These features enable realistic benchmarking for tasks such as chromatin accessibility quantitative trait locus (caQTL) mapping. simPIC generates data that closely match real datasets and better captures inter-individual and experimental variation compared to existing tools.

Indexed as

simulationsingle-cell ATAC-seqsingle-cell genomicssoftware package

Identifiers

PMID41040405
PMCPMC12485805

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.