Peter Ebert
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Explore the profile of Peter Ebert including associated specialties, affiliations and a list of published articles.
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36
Citations
1631
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Recent Articles
1.
Snyder T, Gittelman R, Klinger M, May D, Osborne E, Taniguchi R, et al.
Front Immunol
. 2025 Jan;
15():1488860.
PMID: 39840037
Introduction: T cells are involved in the early identification and clearance of viral infections and also support the development of antibodies by B cells. This central role for T cells...
2.
Henglin M, Ghareghani M, Harvey W, Porubsky D, Koren S, Eichler E, et al.
Genome Biol
. 2024 Oct;
25(1):265.
PMID: 39390579
Haplotype information is crucial for biomedical and population genetics research. However, current strategies to produce de novo haplotype-resolved assemblies often require either difficult-to-acquire parental data or an intermediate haplotype-collapsed assembly....
3.
Logsdon G, Ebert P, Audano P, Loftus M, Porubsky D, Ebler J, et al.
bioRxiv
. 2024 Oct;
PMID: 39372794
Diverse sets of complete human genomes are required to construct a pangenome reference and to understand the extent of complex structural variation. Here, we sequence 65 diverse human genomes and...
4.
Porubsky D, Dashnow H, Sasani T, Logsdon G, Hallast P, Noyes M, et al.
bioRxiv
. 2024 Aug;
PMID: 39149261
Using five complementary short- and long-read sequencing technologies, we phased and assembled >95% of each diploid human genome in a four-generation, 28-member family (CEPH 1463) allowing us to systematically assess...
5.
Henglin M, Ghareghani M, Harvey W, Porubsky D, Koren S, Eichler E, et al.
bioRxiv
. 2024 Mar;
PMID: 38529499
Haplotype information is crucial for biomedical and population genetics research. However, current strategies to produce haplotype-resolved assemblies often require either difficult-to-acquire parental data or an intermediate haplotype-collapsed assembly. Here, we...
6.
Harvey W, Ebert P, Ebler J, Audano P, Munson K, Hoekzema K, et al.
Genome Res
. 2024 Jan;
33(12):2029-2040.
PMID: 38190646
Advances in long-read sequencing (LRS) technologies continue to make whole-genome sequencing more complete, affordable, and accurate. LRS provides significant advantages over short-read sequencing approaches, including phased de novo genome assembly,...
7.
Hallast P, Ebert P, Loftus M, Yilmaz F, Audano P, Logsdon G, et al.
Nature
. 2023 Aug;
621(7978):355-364.
PMID: 37612510
The prevalence of highly repetitive sequences within the human Y chromosome has prevented its complete assembly to date and led to its systematic omission from genomic analyses. Here we present...
8.
Keitany G, Rubin B, Garrett M, Musa A, Tracy J, Liang Y, et al.
Cell Chem Biol
. 2023 Aug;
30(11):1377-1389.e8.
PMID: 37586370
TruAB Discovery is an approach that integrates cellular immunology, high-throughput immunosequencing, bioinformatics, and computational biology in order to discover naturally occurring human antibodies for prophylactic or therapeutic use. We adapted...
9.
Maji R, Czepukojc B, Scherer M, Tierling S, Cadenas C, Gianmoena K, et al.
Epigenetics Chromatin
. 2023 Jul;
16(1):30.
PMID: 37415213
Fatty liver disease or the accumulation of fat in the liver, has been reported to affect the global population. This comes with an increased risk for the development of fibrosis,...
10.
Harvey W, Ebert P, Ebler J, Audano P, Munson K, Hoekzema K, et al.
bioRxiv
. 2023 May;
PMID: 37205567
Advances in long-read sequencing (LRS) technology continue to make whole-genome sequencing more complete, affordable, and accurate. LRS provides significant advantages over short-read sequencing approaches, including phased genome assembly, access to...