Author

Carolyn M. Millar

Imperial College Healthcare NHS Trust

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1

Frequent Co-Authors

Aarnoud P. HuissooniD· 1 shared Abigail Furnell· 1 shared Adam J. MeadiD· 1 shared Adam P. LevineiD· 1 shared Adnan Yousaf Manzur· 1 shared Adrian James ThrasheriD· 1 shared Alan J. Greenhalgh· 1 shared Alasdair P. J. ParkeriD· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperBioinformatics

Aarnoud P. HuissoonORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintAug 28, 2021

High definition analyses of single cohort, whole genome sequencing data provides a direct route to defining sub-phenotypes and personalising medicine

Katie E. Joyce, Ebun Onabanjo, Sheila Brownlow…·Claire L. Shovlin

The paper analyzes whole genome sequencing data from endothelial vasculopathy patients to identify rare variants in clinically relevant genes and their association with disease severity.

DOI 10.1101/2021.08.28.21262560

humanwhole-genome sequencing

𝕏 PostBluesky

BioinformaticsScientific ReportsPeer-reviewedJan 16, 2018

Telomerecat: A Ploidy-Agnostic Method For Estimating Telomere Length From Whole Genome Sequencing Data

James H. R. Farmery, Mike L. Smith, NIHR BioResource - Rare Diseases…·Emma L. Wakeling

Telomerecat estimates telomere length from whole-genome sequencing data without requiring prior knowledge of ploidy, showing good performance and detecting expected patterns in various data types.

88 citationstop 2%

whole-genome sequencingstatistical model

𝕏 PostBluesky