Evidence map›Paper›PMID 37473732›Full record

ArticleCell systems2023

SiftCell: A robust framework to detect and isolate cell-containing droplets from single-cell RNA sequence reads.

Jingyue Xi, Sung Rye Park, Jun Hee Lee, Hyun Min Kang

Abstract read
In one paragraph

Article in Cell systems, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. A who's who of cell types in skeletal muscle.Communications biology · 2026
    Review
  2. Review
  3. Review
  4. Article
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

4 authors.

Jingyue XiDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan, Ann Arbor, MI 48109-2029, USA.
Sung Rye ParkDepartment of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48109-2200, USA.
Jun Hee LeeDepartment of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48109-2200, USA.
Hyun Min KangDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan, Ann Arbor, MI 48109-2029, USA. Electronic address: hmkang@umich.edu.

Funding

Mechanisms underlying Hepatoprotective Roles of Sestrin2R01DK102850 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEE, JUN HEE · 2015 to 2019
$1.7M
Scalable and Translational Analysis Tools on the Cloud for Deep Integrative Omics DataU01HL137182 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHOU, XIANG · 2017 to 2019
$1.6M
Leveraging long-range haplotypes in sequencing data to advance large scale genetic studiesR01HG011031 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZOELLNER, SEBASTIAN · 2020 to 2023
$1.4M
Seq-Scope: Microscopic Examination of Spatial Single Cell Transcriptome in Cell and Tissue SenescenceUG3CA268091 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEE, JUN HEE · 2021 to 2022
$1.1M
Protein inclusions in non-alcoholic steatohepatitisR01DK114131 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEE, JUN HEE · 2018 to 2020
$1.0M
NCI NIH HHS UG3 CA268091NHGRI NIH HHS R01 HG011031NHLBI NIH HHS U01 HL137182NIDDK NIH HHS R01 DK102850NIDDK NIH HHS R01 DK114131
6 · The paper itself

Abstract

Single-cell RNA sequencing (scRNA-seq) massively profiles transcriptomes of individual cells encapsulated in barcoded droplets in parallel. However, in real-world scRNA-seq data, many barcoded droplets do not contain cells, but instead, they capture a fraction of ambient RNAs released from damaged or lysed cells. A typical first step to analyze scRNA-seq data is to filter out cell-free droplets and isolate cell-containing droplets, but distinguishing them is often challenging; incorrect filtering may mislead the downstream analysis substantially. We propose SiftCell, a suite of software tools to identify and visualize cell-containing and cell-free droplets in manifold space via randomization (SiftCell-Shuffle) to classify between the two types of droplets (SiftCell-Boost) and to quantify the contribution of ambient RNAs for each droplet (SiftCell-Mix). By applying our method to datasets obtained by various single-cell platforms, we show that SiftCell provides a streamlined way to perform upstream quality control of scRNA-seq, which is more comprehensive and accurate than existing methods.

Indexed as

Single-Cell AnalysisSoftwareBase SequenceRNARNA-SeqSequence Analysis, RNARNAambient RNAcRNA-seqsingle celltranscriptomics

Identifiers

PMID37473732
PMCPMC10411962

What OpenQuestion holds

Textmetadata
LicenceTDM
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.