FRITZ SEDLAZECK to Computational Biology
This is a "connection" page, showing publications FRITZ SEDLAZECK has written about Computational Biology.
Connection Strength
2.803
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Computational analysis of DNA methylation from long-read sequencing. Nat Rev Genet. 2025 Sep; 26(9):620-634.
Score: 0.633
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Towards population-scale long-read sequencing. Nat Rev Genet. 2021 09; 22(9):572-587.
Score: 0.485
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PhaseME: Automatic rapid assessment of phasing quality and phasing improvement. Gigascience. 2020 07 01; 9(7).
Score: 0.456
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Piercing the dark matter: bioinformatics of long-range sequencing and mapping. Nat Rev Genet. 2018 06; 19(6):329-346.
Score: 0.394
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Closing the gaps, and improving somatic structural variant analysis and benchmarking using CHM13-T2T. Genome Res. 2025 Apr 14; 35(4):621-631.
Score: 0.159
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A Hitchhiker's Guide to long-read genomic analysis. Genome Res. 2025 Apr 14; 35(4):545-558.
Score: 0.159
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Unveiling microbial diversity: harnessing long-read sequencing technology. Nat Methods. 2024 Jun; 21(6):954-966.
Score: 0.149
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A multi-task convolutional deep neural network for variant calling in single molecule sequencing. Nat Commun. 2019 03 01; 10(1):998.
Score: 0.104
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GenomeScope: fast reference-free genome profiling from short reads. Bioinformatics. 2017 Jul 15; 33(14):2202-2204.
Score: 0.093
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Benefit-of-doubt (BOD) scoring: a sequencing-based method for SNP candidate assessment from high to medium read number data sets. Genomics. 2013 Mar; 101(3):204-9.
Score: 0.067
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Unraveling the hidden complexity of cancer through long-read sequencing. Genome Res. 2025 Apr 14; 35(4):599-620.
Score: 0.040
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Genomic variant benchmark: if you cannot measure it, you cannot improve it. Genome Biol. 2023 10 05; 24(1):221.
Score: 0.036
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muCNV: Genotyping Structural Variants for Population-level Sequencing. Bioinformatics. 2021 08 04; 37(14):2055?2057.
Score: 0.030