FRITZ SEDLAZECK to Base Sequence
This is a "connection" page, showing publications FRITZ SEDLAZECK has written about Base Sequence.
Connection Strength
0.481
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Hidden biases in germline structural variant detection. Genome Biol. 2021 12 20; 22(1):347.
Score: 0.141
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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: 0.116
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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: 0.075
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The complete sequence of a human Y chromosome. Nature. 2023 Sep; 621(7978):344-354.
Score: 0.040
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Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome. Nat Biotechnol. 2019 10; 37(10):1155-1162.
Score: 0.030
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Decreased expression of endogenous feline leukemia virus in cat lymphomas: a case control study. BMC Vet Res. 2015 Apr 10; 11:90.
Score: 0.022
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ADAR2 induces reproducible changes in sequence and abundance of mature microRNAs in the mouse brain. Nucleic Acids Res. 2014 Oct 29; 42(19):12155-68.
Score: 0.021
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Advanced methylome analysis after bisulfite deep sequencing: an example in Arabidopsis. PLoS One. 2012; 7(7):e41528.
Score: 0.018
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Adenosine deaminases that act on RNA induce reproducible changes in abundance and sequence of embryonic miRNAs. Genome Res. 2012 Aug; 22(8):1468-76.
Score: 0.018