FRITZ SEDLAZECK to Genomics
This is a "connection" page, showing publications FRITZ SEDLAZECK has written about Genomics.
Connection Strength
6.618
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A Hitchhiker's Guide to long-read genomic analysis. Genome Res. 2025 04 14; 35(4):545-558.
Score: 0.505
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Comprehensive genome analysis and variant detection at scale using DRAGEN. Nat Biotechnol. 2025 Jul; 43(7):1177-1191.
Score: 0.489
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Analysis and benchmarking of small and large genomic variants across tandem repeats. Nat Biotechnol. 2025 Mar; 43(3):431-442.
Score: 0.472
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FixItFelix: improving genomic analysis by fixing reference errors. Genome Biol. 2023 02 21; 24(1):31.
Score: 0.435
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Hidden biases in germline structural variant detection. Genome Biol. 2021 12 20; 22(1):347.
Score: 0.401
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Towards population-scale long-read sequencing. Nat Rev Genet. 2021 09; 22(9):572-587.
Score: 0.386
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Parliament2: Accurate structural variant calling at scale. Gigascience. 2020 12 21; 9(12).
Score: 0.374
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PhaseME: Automatic rapid assessment of phasing quality and phasing improvement. Gigascience. 2020 07 01; 9(7).
Score: 0.362
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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: 0.314
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NextGenMap: fast and accurate read mapping in highly polymorphic genomes. Bioinformatics. 2013 Nov 01; 29(21):2790-1.
Score: 0.225
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Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications. Genome Res. 2026 Mar 02; 36(3):460-471.
Score: 0.134
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VACmap: an accurate long-read aligner for unraveling complex genomic rearrangements. Nat Commun. 2026 Jan 05; 16(1):11198.
Score: 0.133
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GREGoR: accelerating genomics for rare diseases. Nature. 2025 11; 647(8089):331-342.
Score: 0.131
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Unraveling the hidden complexity of cancer through long-read sequencing. Genome Res. 2025 04 14; 35(4):599-620.
Score: 0.126
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K-mer analysis of long-read alignment pileups for structural variant genotyping. Nat Commun. 2025 Apr 04; 16(1):3218.
Score: 0.126
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The GIAB genomic stratifications resource for human reference genomes. Nat Commun. 2024 10 19; 15(1):9029.
Score: 0.122
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When less is more: sketching with minimizers in genomics. Genome Biol. 2024 Oct 14; 25(1):270.
Score: 0.122
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Impact and characterization of serial structural variations across humans and great apes. Nat Commun. 2024 09 13; 15(1):8007.
Score: 0.121
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Improved sequence mapping using a complete reference genome and lift-over. Nat Methods. 2024 Jan; 21(1):41-49.
Score: 0.115
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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: 0.114
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The complete sequence of a human Y chromosome. Nature. 2023 09; 621(7978):344-354.
Score: 0.113
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Multiscale analysis of pangenomes enables improved representation of genomic diversity for repetitive and clinically relevant genes. Nat Methods. 2023 08; 20(8):1213-1221.
Score: 0.111
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Inference of phylogenetic trees directly from raw sequencing reads using Read2Tree. Nat Biotechnol. 2024 Jan; 42(1):139-147.
Score: 0.110
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Multiple genome alignment in the telomere-to-telomere assembly era. Genome Biol. 2022 08 29; 23(1):182.
Score: 0.105
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A complete reference genome improves analysis of human genetic variation. Science. 2022 04; 376(6588):eabl3533.
Score: 0.102
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Fully resolved assembly of Cryptosporidium parvum. Gigascience. 2022 02 15; 11.
Score: 0.101
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Structural variant calling: the long and the short of it. Genome Biol. 2019 11 20; 20(1):246.
Score: 0.087
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RaGOO: fast and accurate reference-guided scaffolding of draft genomes. Genome Biol. 2019 10 28; 20(1):224.
Score: 0.086
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Accurate detection of complex structural variations using single-molecule sequencing. Nat Methods. 2018 06; 15(6):461-468.
Score: 0.078
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The genomic basis of circadian and circalunar timing adaptations in a midge. Nature. 2016 12 01; 540(7631):69-73.
Score: 0.071
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Phased diploid genome assembly with single-molecule real-time sequencing. Nat Methods. 2016 Dec; 13(12):1050-1054.
Score: 0.070
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Teaser: Individualized benchmarking and optimization of read mapping results for NGS data. Genome Biol. 2015 Oct 22; 16:235.
Score: 0.065
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Complete genomic characterization of global pathogens respiratory syntical virus and human norovirus using probe based capture enrichment. Sci Rep. 2025 Jul 01; 15(1):20526.
Score: 0.032
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Small variant benchmark from a complete assembly of X and Y chromosomes. Nat Commun. 2025 Jan 08; 16(1):497.
Score: 0.031
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StratoMod: predicting sequencing and variant calling errors with interpretable machine learning. Commun Biol. 2024 10 13; 7(1):1316.
Score: 0.030
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De Novo Genome Assembly for the Coppery Titi Monkey (Plecturocebus cupreus): An Emerging Nonhuman Primate Model for Behavioral Research. Genome Biol Evol. 2024 05 02; 16(5).
Score: 0.030
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Variant calling and benchmarking in an era of complete human genome sequences. Nat Rev Genet. 2023 07; 24(7):464-483.
Score: 0.027
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The EN-TEx resource of multi-tissue personal epigenomes?& variant-impact models. Cell. 2023 03 30; 186(7):1493-1511.e40.
Score: 0.027
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The third international hackathon for applying insights into large-scale genomic composition to use cases in a wide range of organisms. F1000Res. 2022; 11:530.
Score: 0.026
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Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment. Gigascience. 2021 09 24; 10(9).
Score: 0.025
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Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes. Nat Biotechnol. 2020 09; 38(9):1044-1053.
Score: 0.022
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A Genocentric Approach to Discovery of Mendelian Disorders. Am J Hum Genet. 2019 11 07; 105(5):974-986.
Score: 0.022
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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: 0.021
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The pineapple genome and the evolution of CAM photosynthesis. Nat Genet. 2015 Dec; 47(12):1435-42.
Score: 0.016