Evidence map›Paper›PMID 37258906›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

Protocol for Classification Single-Cell PBMC Types from Pathological Samples Using Supervised Machine Learning.

Minjie Lyu, Lin Xin, Huan Jin, Lou T Chitkushev, Guanglan Zhang, Derin B Keskin, Vladimir Brusic

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Minjie LyuSchool of Computer Science, University of Nottingham, Ningbo, Zhejiang, China.
Lin XinSchool of Computer Science, University of Nottingham, Ningbo, Zhejiang, China.
Huan JinSchool of Computer Science, University of Nottingham, Ningbo, Zhejiang, China.
Lou T ChitkushevDepartment of Computer Science, Metropolitan College, Boston University, Boston, MA, USA.
Guanglan ZhangDepartment of Computer Science, Metropolitan College, Boston University, Boston, MA, USA.
Derin B KeskinTranslational Immuno-Genomics Lab, Dana-Farber Cancer Institute, Boston, MA, USA.
Vladimir BrusicSchool of Computer Science, University of Nottingham, Ningbo, Zhejiang, China. vladimir.brusic@nottingham.edu.cn.

Funding

Treating the P13-Kinase/AKTP50CA101942 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI David McDermott · 2003 to 2026
$53.4M
Physical detection of HLA-C binding peptides to identify and predict immunogenic personal neoepitopes for improving cancer vaccinesR21CA216772 · NCI · DANA-FARBER CANCER INST · PI KESKIN, DERIN B · 2018 to 2019
$420k
NCI NIH HHS P50 CA101942NCI NIH HHS R21 CA216772
6 · The paper itself

Abstract

Peripheral blood mononuclear cells (PBMC) are mixed subpopulations of blood cells composed of five cell types. PBMC are widely used in the study of the immune system, infectious diseases, cancer, and vaccine development. Single-cell transcriptomics (SCT) allows the labeling of cell types by gene expression patterns from biological samples. Classifying cells into cell types and states is essential for single-cell analyses, especially in the classification of diseases and the assessment of therapeutic interventions, and for many secondary analyses. Most of the classification of cell types from SCT data use unsupervised clustering or a combination of unsupervised and supervised methods including manual correction. In this chapter, we describe a protocol that uses supervised machine learning (ML) methods with SCT data for the classification of PBMC cell types in samples representing pathological states. This protocol has three parts: (1) data preprocessing, (2) labeling of reference PBMC SCT datasets and training supervised ML models, and (3) labeling new PBMC datasets from disease samples. This protocol enables building classification models that are of high accuracy and efficiency. Our example focuses on 10× Genomics technology but applies to datasets from other SCT platforms.

Indexed as

Leukocytes, MononuclearNeoplasmsGene Expression ProfilingGenomicsHumansSupervised Machine LearningCell type classificationDiseasePeripheral blood mononuclear cellsProtocolSingle-cell transcriptomicsSupervised machine learning

Identifiers

What Socratic holds

Textmetadata
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.