Evidence map›Paper›PMID 27897010›Full record

ArticlePacific Symposium on Biocomputing. Pacific Symposium on Biocomputing2017

MAPPING NEURONAL CELL TYPES USING INTEGRATIVE MULTI-SPECIES MODELING OF HUMAN AND MOUSE SINGLE CELL RNA SEQUENCING.

Travis Johnson, Zachary Abrams, Yan Zhang, Kun Huang

Abstract read
In one paragraph

Article in Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

Travis JohnsonDept. Biomedical Informatics, Ohio State University, 250 Lincoln Tower, 1800 Cannon Dr. Columbus, 43210, Ohio, USA, Travis.Johnson@osumc.edu.
Zachary Abrams
Yan Zhang
Kun Huang

Funding

The OSU Clinical and Translational Research Informatics Training Program (CTRIP)T15LM011270 · NLM · OHIO STATE UNIVERSITY · PI COOMBES, KEVIN ROBERT, JANIES, DANIEL A. · 2012 to 2016
$2.2M
NLM NIH HHS T15 LM011270
6 · The paper itself

Abstract

Mouse brain transcriptomic studies are important in the understanding of the structural heterogeneity in the brain. However, it is not well understood how cell types in the mouse brain relate to human brain cell types on a cellular level. We propose that it is possible with single cell granularity to find concordant genes between mouse and human and that these genes can be used to separate cell types across species. We show that a set of concordant genes can be algorithmically derived from a combination of human and mouse single cell sequencing data. Using this gene set, we show that similar cell types shared between mouse and human cluster together. Furthermore we find that previously unclassified human cells can be mapped to the glial/vascular cell type by integrating mouse cell type expression profiles.

Indexed as

AlgorithmsAnimalsBrainComputational BiologyGene Expression ProfilingHumansMiceModels, NeurologicalMultigene FamilyNeuronsSequence Analysis, RNASpecies Specificity

Identifiers

PMID27897010
PMCPMC6956653

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.