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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2023 | 1 |
2024 | 3 |
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4 results
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Page 1
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation.
medRxiv [Preprint]. 2024 Mar 7:2024.03.05.24303792. doi: 10.1101/2024.03.05.24303792.
medRxiv. 2024.
PMID: 38496498
Free PMC article.
Preprint.
The benefit of a complete reference genome for cancer structural variant analysis.
Paulin LF, Fan J, O'Neill K, Pleasance E, Porter VL, Jones SJM, Sedlazeck FJ.
Paulin LF, et al.
medRxiv [Preprint]. 2024 Mar 18:2024.03.15.24304369. doi: 10.1101/2024.03.15.24304369.
medRxiv. 2024.
PMID: 38562786
Free PMC article.
Preprint.
Item in Clipboard
Publisher Correction: Detection of mosaic and population-level structural variants with Sniffles2.
Smolka M, Paulin LF, Grochowski CM, Horner DW, Mahmoud M, Behera S, Kalef-Ezra E, Gandhi M, Hong K, Pehlivan D, Scholz SW, Carvalho CMB, Proukakis C, Sedlazeck FJ.
Smolka M, et al.
Nat Biotechnol. 2024 Jan 22. doi: 10.1038/s41587-024-02141-2. Online ahead of print.
Nat Biotechnol. 2024.
PMID: 38253882
No abstract available.
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Single-cell somatic copy number variants in brain using different amplification methods and reference genomes.
Kalef-Ezra E, Turan ZG, Perez-Rodriguez D, Bomann I, Behera S, Morley C, Scholz SW, Jaunmuktane Z, Demeulemeester J, Sedlazeck FJ, Proukakis C.
Kalef-Ezra E, et al.
bioRxiv [Preprint]. 2023 Nov 21:2023.08.07.552289. doi: 10.1101/2023.08.07.552289.
bioRxiv. 2023.
PMID: 37609320
Free PMC article.
Preprint.
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