Mitchell R Vollger
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Explore the profile of Mitchell R Vollger including associated specialties, affiliations and a list of published articles.
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34
Citations
4375
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Recent Articles
1.
Vollger M, Korlach J, Eldred K, Swanson E, Underwood J, Bohaczuk S, et al.
Nat Genet
. 2025 Jan;
57(2):469-479.
PMID: 39880924
Resolving the molecular basis of a Mendelian condition remains challenging owing to the diverse mechanisms by which genetic variants cause disease. To address this, we developed a synchronized long-read genome,...
2.
Bohaczuk S, Amador Z, Li C, Mallory B, Swanson E, Ranchalis J, et al.
Genome Res
. 2024 Dec;
34(12):2269-2278.
PMID: 39653420
Accurately quantifying the functional consequences of noncoding mosaic variants requires the pairing of DNA sequences with both accessible and closed chromatin architectures along individual DNA molecules-a pairing that cannot be...
3.
Peter C, Agarwal A, Watanabe R, Kassim B, Wang X, Lambert T, et al.
Cell Rep Methods
. 2024 Dec;
4(12):100911.
PMID: 39631398
We apply a single-molecule chromatin fiber sequencing (Fiber-seq) protocol designed for amplification-free cell-type-specific mapping of the regulatory architecture at nucleosome resolution along extended ∼10-kb chromatin fibers to neuronal and non-neuronal...
4.
Bohaczuk S, Amador Z, Li C, Mallory B, Swanson E, Ranchalis J, et al.
bioRxiv
. 2024 Jul;
PMID: 39026856
Accurately quantifying the functional consequences of non-coding mosaic variants requires the pairing of DNA sequence with both accessible and closed chromatin architectures along individual DNA molecules-a pairing that cannot be...
5.
Bubb K, Hamm M, Tullius T, Min J, Ramirez-Corona B, Mueth N, et al.
bioRxiv
. 2024 Jul;
PMID: 39026747
The genomes of flowering plants consist largely of transposable elements (TEs), some of which modulate gene regulation and function. However, the repetitive nature of TEs and difficulty of mapping individual...
6.
Jha A, Bohaczuk S, Mao Y, Ranchalis J, Mallory B, Min A, et al.
Genome Res
. 2024 Jun;
34(11):1976-1986.
PMID: 38849157
Long-read DNA sequencing has recently emerged as a powerful tool for studying both genetic and epigenetic architectures at single-molecule and single-nucleotide resolution. Long-read epigenetic studies encompass both the direct identification...
7.
Grasberger H, Dumitrescu A, Liao X, Swanson E, Weiss R, Srichomkwun P, et al.
Nat Genet
. 2024 May;
56(5):877-888.
PMID: 38714869
Thyrotropin (TSH) is the master regulator of thyroid gland growth and function. Resistance to TSH (RTSH) describes conditions with reduced sensitivity to TSH. Dominantly inherited RTSH has been linked to...
8.
Vollger M, Korlach J, Eldred K, Swanson E, Underwood J, Cheng Y, et al.
bioRxiv
. 2023 Oct;
PMID: 37808736
Resolving the molecular basis of a Mendelian condition (MC) remains challenging owing to the diverse mechanisms by which genetic variants cause disease. To address this, we developed a synchronized long-read...
9.
Rhie A, Nurk S, Cechova M, Hoyt S, Taylor D, Altemose N, et al.
Nature
. 2023 Aug;
621(7978):344-354.
PMID: 37612512
The human Y chromosome has been notoriously difficult to sequence and assemble because of its complex repeat structure that includes long palindromes, tandem repeats and segmental duplications. As a result,...
10.
Yang X, Wang X, Zou Y, Zhang S, Xia M, Fu L, et al.
Genome Biol
. 2023 Jul;
24(1):157.
PMID: 37403156
Background: The first telomere-to-telomere (T2T) human genome assembly (T2T-CHM13) release is a milestone in human genomics. The T2T-CHM13 genome assembly extends our understanding of telomeres, centromeres, segmental duplication, and other...