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Record W2592790535 · doi:10.1101/107573

Duplication events downstream of <i>IRX1</i> cause North Carolina macular dystrophy at the MCDR3 locus

2017· preprint· en· W2592790535 on OpenAlexaff
Valentina Cipriani, Raquel Sofia Silva, Gavin Arno, Nikolas Pontikos, Ambreen Kalhoro, Sandra Valeiņa, Inna Inashkina, Māreta Audere, Katrīna Rutka, Bernard Puech, Michel Michaelides, Veronica van Heyningen, Baiba Lāce, Andrew R. Webster, Anthony T. Moore

Bibliographic record

VenuebioRxiv (Cold Spring Harbor Laboratory) · 2017
Typepreprint
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicRetinal Development and Disorders
Canadian institutionsCentre hospitalier de l'Université Laval
FundersNIHR BioResourceMoorfields Eye CharityMoorfields Eye Hospital NHS Foundation TrustFoundation Fighting BlindnessUniversity Hospitals of Leicester NHS TrustMacular SocietyNational Institute for Health and Care ResearchResearch to Prevent Blindness
KeywordsGeneticsBiologyLocus (genetics)Gene duplicationHaplotypeCopy-number variationSingle-nucleotide polymorphismGeneGenomeGenotype

Abstract

fetched live from OpenAlex

Abstract Autosomal dominant North Carolina macular dystrophy (NCMD) is believed to represent a failure of macular development. The disorder has been assigned by linkage to two loci, MCDR1 on chromosome 6q16 and MCDR3 on chromosome 5p15-p13. Recently, noncoding variants upstream of PRDM13 and a large duplication including IRX1 have been identified. However, the underlying disease-causing mechanism remains uncertain. Through a combination of sequencing studies, we report two novel overlapping duplications at the MCDR3 locus, in a gene desert downstream of IRX1 and upstream of ADAMTS16. One duplication of 43 kb was identified in nine NCMD families (with evidence for a shared ancestral haplotype), and another one of 45 kb was found in a single family. The MCDR3 locus is thus refined to a shared region of 39 kb that contains DNAse hypersensitive sites active at a restricted time window during retinal development. Publicly available data confirmed expression of IRX1 and ADAMTS16 in human fetal retina, with IRX1 preferentially expressed in fetal macula. These findings represent a major advance in our understanding of the molecular genetics of NCMD at the MCDR3 locus and provide insights into the genetic pathways involved in human macular development. Abbreviations list aCGH array comparative genomic hybridization CNV Copy number variant IBD Identical-by-descent iPSC Induced pluripotent stem cell DHS DNase hypersensitive site HH Homozygosity Haplotype MCDR Macular dystrophy region NCMD North Carolina macular dystrophy PCR Polymerase chain reaction RCHH Region with a Conserved Homozygosity Haplotype SNP Single-nucleotide polymorphism SNV Single nucleotide variant SV Structural variant WGS Whole-genome sequencing

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
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 score0.201
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

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 head0.009
GPT teacher head0.217
Teacher spread0.209 · 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 teacher head, not a consensus.

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
Published2017
Admission routes1
Has abstractyes

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