Evidence map›Paper›PMID 30530777›Full record

ArticleBlood advances2018

CapTCR-seq: hybrid capture for T-cell receptor repertoire profiling.

David T Mulder, Etienne R Mahé, Mark Dowar, Youstina Hanna, Tiantian Li, Linh T Nguyen, Marcus O Butler, Naoto Hirano, Jan Delabie, Pamela S Ohashi and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Blood advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.8field-weighted citation impact, top 24% of its field
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

16 citing papers in PubMed, 25 citations in OpenAlex.

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  8. Efficacy of Nivolumab in Pediatric Cancers with High Mutation Burden and Mismatch Repair Deficiency.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

David T MulderPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Etienne R MahéDivision of Hematology, Calgary Laboratory Services and Department of Pathology and Laboratory Medicine, University of Calgary, Calgary, AB, Canada.ORCID 0000-0002-6559-9339
Mark DowarPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Youstina HannaPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Tiantian LiPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Linh T NguyenPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Marcus O ButlerPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Naoto HiranoPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Jan DelabieLaboratory Medicine Program, University Health Network, Toronto, ON, Canada; and.
Pamela S OhashiPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Trevor J PughPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.ORCID 0000-0002-8073-5888
University Health Network · CAOntario Institute for Cancer Research · CAUniversity of Calgary · CA

Funding

CIHR
6 · The paper itself

Abstract

Mature T-cell lymphomas consisting of an expanded clonal population of T cells that possess common rearrangements of the T-cell receptor (TCR) encoding genes can be identified and monitored using molecular methods of T-cell repertoire analysis. We have developed a hybrid-capture method that enriches DNA sequencing libraries for fragments encoding rearranged TCR genes from all 4 loci in a single reaction. We use this method to describe the TCR repertoires of 63 putative lymphoma clinical isolates, 7 peripheral blood mononuclear cell (PBMC) populations, and a collection of tumor infiltrating lymphocytes. Dominant Variable (V) and Joining (J) gene pair rearrangements in cancer cells were confirmed by polymerase chain reaction (PCR) amplification and Sanger sequencing; clonality assessment of clinical isolates using BIOMED-2 methods showed agreement for 73% and 77% of samples at the β and γ loci, respectively, whereas β locus V and J allele prevalence in PBMCs were well correlated with results from commercial PCR-based DNA sequencing assays (

Indexed as

Gene LibraryGene Rearrangement, T-LymphocyteGenetic LociHumansLeukocytes, MononuclearLymphoma, T-CellPolymerase Chain ReactionReceptors, Antigen, T-Cell, alpha-betaReceptors, Antigen, T-Cell, gamma-deltaSequence Analysis, DNAReceptors, Antigen, T-Cell, alpha-betaReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID30530777
PMCPMC6290103
OpenAlexW2904522373

What OpenQuestion 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 OpenQuestion graph.