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Record W6991422799

Genome-wide identification of novel regions of DNA copy number alterations in natural killer cell lymphoma by array comparative genomic hybridization

2010· other· en· W6991422799 on OpenAlexaboutno aff

Bibliographic record

VenueThe HKU Scholars Hub (University of Hong Kong) · 2010
Typeother
Languageen
FieldMedicine
TopicClinical practice guidelines implementation
Canadian institutionsnot available
Fundersnot available
KeywordsComparative genomic hybridizationGenomeCopy number analysisLymphomaNatural killer cellHuman genomeCopy-number variationChromosomeGene
DOInot available

Abstract

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Introduction: Natural killer (NK) cell lymphoma encompasses a related spectrum of diseases and is among the most aggressive of all lymphoid malignancies. The nasal type is characterized by necrotic lesions in the nasal cavity, nasopharynx, or palate, whereas patients suffering from the aggressive type might die within a short time from disseminated disease or multi-organ failure. It is a relatively rare disease and is generally more common in Asians than in other races. Since it has not been well characterized until recently, the identification of genetic alterations would provide important insights into the genomic mechanism of lymphomagenesis. Hypotheses: NK cell lymphoma pathogenesis occurs via multiple genomic alterations and the critical alterations will be present in multiple NK cell lines. Objective: Alignment of high resolution genomic profiles from multiple NK cell lines will reveal minimal regions of alteration important in the pathogenesis of NK-cell lymphoma. Experimental Approach: To determine segmental DNA copy number changes across an entire genome, whole genome tiling path array is employed to evaluate segmental DNA gains and losses which may contain oncogenes and tumor suppressors. Currently, the whole genome has been arrayed as 26,819 bacterial artificial chromosome (BAC) derived amplified fragment pools spotted in duplicate (53,638 elements) resulting in tiling resolution with complete coverage of the sequenced human genome. Results: Whole genome array CGH was used to generate high resolution segmental copy number profiles of seven NK cell lymphoma cell lines (HANK1, KHYG-1, NK-92, NK-YS, SNK1, SNK6, and KAI3). Alignment of these profiles with the human genome map has resulted in fine-mapping the regional losses of 6q. Numerous novel regions, including gain of 5p15.33, and loss of 4q21.23-q32.1, 9p21.1-p22.3, and 12q24.32-q24.33 were also identified in at least five (>70%) of these cell lines. Conclusions: The generation of the high resolution segmental copy number profiles by array CGH allows the identification of genomic alterations of NK-cell lymphomas as well as the candidate genes involved in the pathogenesis of NK-cell lymphoma. Novel candidate oncogenes and tumor suppressor genes identified in this study will provide further insights into the genetic basis of lymphomagenesis. Acknowledgements: This work was supported by funds from Genome Canada/British Columbia. WCC is supported by the Director’s Challenge grant (U01-CA 84967). We would like to thank Spencer Watson for BAC array production and Magan Trottier for technical assistance.

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How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.001
Threshold uncertainty score0.004

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.061
GPT teacher head0.343
Teacher spread0.282 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2010
Admission routes1
Has abstractyes

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