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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2020 | 1 |
2022 | 1 |
2023 | 2 |
2024 | 0 |
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Benchmarking challenging small variants with linked and long reads.
Cell Genom. 2022 May;2(5):100128. doi: 10.1016/j.xgen.2022.100128.
Cell Genom. 2022.
PMID: 36452119
Free PMC article.
A multilocus approach for accurate variant calling in low-copy repeats using whole-genome sequencing.
Prodanov T, Bansal V.
Prodanov T, et al.
Bioinformatics. 2023 Jun 30;39(39 Suppl 1):i279-i287. doi: 10.1093/bioinformatics/btad268.
Bioinformatics. 2023.
PMID: 37387146
Free PMC article.
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HapCUT2: A Method for Phasing Genomes Using Experimental Sequence Data.
Bansal V.
Bansal V.
Methods Mol Biol. 2023;2590:139-147. doi: 10.1007/978-1-0716-2819-5_9.
Methods Mol Biol. 2023.
PMID: 36335497
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Sensitive alignment using paralogous sequence variants improves long-read mapping and variant calling in segmental duplications.
Prodanov T, Bansal V.
Prodanov T, et al.
Nucleic Acids Res. 2020 Nov 4;48(19):e114. doi: 10.1093/nar/gkaa829.
Nucleic Acids Res. 2020.
PMID: 33035301
Free PMC article.
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