Brock A. Peters, Ph.D.
Affiliations: | 2005 | Johns Hopkins University, Baltimore, MD |
Area:
Molecular BiologyGoogle:
"Brock Peters"Parents
Sign in to add mentor| Kenneth W. Kinzler | grad student | 2005 | Johns Hopkins | |
| (Molecular analyses of the transcriptome and angiogenesis.) | ||||
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Publications
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| Cai Y, Anderson E, Xue W, et al. (2024) Assembly and analysis of the genome of Notholithocarpus densiflorus. G3 (Bethesda, Md.) |
| McElwain MA, Peters BA. (2022) Accurate Sequencing and Haplotyping from 10 Cells Using Long Fragment Read (LFR) Technology. Methods in Molecular Biology (Clifton, N.J.). 2590: 71-84 |
| Xu M, Guo L, Gu S, et al. (2020) TGS-GapCloser: A fast and accurate gap closer for large genomes with low coverage of error-prone long reads. Gigascience. 9 |
| Weng J, Chen T, Xie Y, et al. (2020) IterCluster: a barcode clustering algorithm for long fragment read analysis. Peerj. 8: e8431 |
| Liu C, Wang M, Wei X, et al. (2019) An ATAC-seq atlas of chromatin accessibility in mouse tissues. Scientific Data. 6: 65 |
| Wang O, Chin R, Cheng X, et al. (2019) Efficient and unique co-barcoding of second-generation sequencing reads from long DNA molecules enabling cost effective and accurate sequencing, haplotyping, and de novo assembly. Genome Research |
| Hoehe MR, Herwig R, Mao Q, et al. (2019) Significant abundance of cis configurations of coding variants in diploid human genomes. Nucleic Acids Research |
| Walker RF, Ciotlos S, Mao Q, et al. (2018) Clinical and genetic analysis of a rare syndrome associated with neoteny. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 20: 495-502 |
| Mao Q, Chin R, Xie W, et al. (2018) Advanced Whole-Genome Sequencing and Analysis of Fetal Genomes from Amniotic Fluid. Clinical Chemistry |
| Mitropoulos K, Merkouri Papadima E, Xiromerisiou G, et al. (2017) Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients. Human Genomics. 11: 30 |