Evidence map›Paper›PMID 35688990›Full record

ArticleCommunications biology2022

LSH-GAN enables in-silico generation of cells for small sample high dimensional scRNA-seq data.

Snehalika Lall, Sumanta Ray, Sanghamitra Bandyopadhyay

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Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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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

7 citing papers in PubMed.

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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.

Snehalika LallMachine Intelligence Unit, Indian Statistical Institute, Kolkata, West Bengal, 700108, India.
Sumanta RayHealth Analytics Network, Pittsburgh, PA, USA. sumanta.ray@aliah.ac.in.ORCID 0000-0002-3371-8516
Sanghamitra BandyopadhyayMachine Intelligence Unit, Indian Statistical Institute, Kolkata, West Bengal, 700108, India. sanghami@isical.ac.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A fundamental problem of downstream analysis of scRNA-seq data is the unavailability of enough cell samples compare to the feature size. This is mostly due to the budgetary constraint of single cell experiments or simply because of the small number of available patient samples. Here, we present an improved version of generative adversarial network (GAN) called LSH-GAN to address this issue by producing new realistic cell samples. We update the training procedure of the generator of GAN using locality sensitive hashing which speeds up the sample generation, thus maintains the feasibility of applying the standard procedures of downstream analysis. LSH-GAN outperforms the benchmarks for realistic generation of quality cell samples. Experimental results show that generated samples of LSH-GAN improves the performance of the downstream analysis such as feature (gene) selection and cell clustering. Overall, LSH-GAN therefore addressed the key challenges of small sample scRNA-seq data analysis.

Indexed as

Single-Cell AnalysisCluster AnalysisHumans

Identifiers

PMID35688990
PMCPMC9187761

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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.