Andrew Carroll
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Explore the profile of Andrew Carroll including associated specialties, affiliations and a list of published articles.
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96
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4456
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Recent Articles
1.
Wagner J, Olson N, McDaniel J, Harris L, Pinto B, Jaspez D, et al.
Nat Commun
. 2025 Jan;
16(1):497.
PMID: 39779690
The sex chromosomes contain complex, important genes impacting medical phenotypes, but differ from the autosomes in their ploidy and large repetitive regions. To enable technology developers along with research and...
2.
Chang T, Chen W, Qu C, Cheng Z, Elsayed A, Pounds S, et al.
J Clin Oncol
. 2024 Dec;
43(8):1039-1041.
PMID: 39715469
No abstract available.
3.
Daniels C, Abdulkadir A, Cleveland M, McDaniel J, Jaspez D, Rubio-Rodriguez L, et al.
bioRxiv
. 2024 Dec;
PMID: 39677813
Somatic mosaicism is an important cause of disease, but mosaic and somatic variants are often challenging to detect because they exist in only a fraction of cells. To address the...
4.
Mastoras M, Asri M, Brambrink L, Hebbar P, Kolesnikov A, Cook D, et al.
bioRxiv
. 2024 Sep;
PMID: 39345401
Accurate genome assemblies are essential for biological research, but even the highest quality assemblies retain errors caused by the technologies used to construct them. Base-level errors are typically fixed with...
5.
Walker G, Carroll A
BJPsych Bull
. 2024 Sep;
:1-4.
PMID: 39291450
In this article, we reflect on factors which may tempt psychiatrists to move from working in the UK to Australia. A comparison between the UK and Australian healthcare systems is...
6.
Siren J, Eskandar P, Ungaro M, Hickey G, Eizenga J, Novak A, et al.
Nat Methods
. 2024 Sep;
21(11):2017-2023.
PMID: 39261641
Pangenomes reduce reference bias by representing genetic diversity better than a single reference sequence. Yet when comparing a sample to a pangenome, variants in the pangenome that are not part...
7.
Park J, Cook D, Chang P, Kolesnikov A, Brambrink L, Mier J, et al.
bioRxiv
. 2024 Sep;
PMID: 39229187
Somatic variant detection is an integral part of cancer genomics analysis. While most methods have focused on short-read sequencing, long-read technologies now offer potential advantages in terms of repeat mapping...
8.
Chang T, Chen W, Qu C, Cheng Z, Hedges D, Elsayed A, et al.
J Clin Oncol
. 2024 Aug;
42(29):3491-3503.
PMID: 39121442
Purpose: Although cure rates for childhood acute lymphoblastic leukemia (ALL) exceed 90%, ALL remains a leading cause of cancer death in children. Half of relapses arise in children initially classified...
9.
Kolesnikov A, Cook D, Nattestad M, Brambrink L, McNulty B, Gorzynski J, et al.
Nat Commun
. 2024 Jul;
15(1):5907.
PMID: 39003259
Long-read sequencing technology has enabled variant detection in difficult-to-map regions of the genome and enabled rapid genetic diagnosis in clinical settings. Rapidly evolving third-generation sequencing platforms like Pacific Biosciences (PacBio)...
10.
Yun T, Cosentino J, Behsaz B, McCaw Z, Hill D, Luben R, et al.
Nat Genet
. 2024 Jul;
56(8):1604-1613.
PMID: 38977853
Although high-dimensional clinical data (HDCD) are increasingly available in biobank-scale datasets, their use for genetic discovery remains challenging. Here we introduce an unsupervised deep learning model, Representation Learning for Genetic...