FRITZ SEDLAZECK to Software
This is a "connection" page, showing publications FRITZ SEDLAZECK has written about Software.
Connection Strength
5.458
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Comprehensive genome analysis and variant detection at scale using DRAGEN. Nat Biotechnol. 2025 Jul; 43(7):1177-1191.
Score: 0.602
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SVhound: detection of regions that harbor yet undetected structural variation. BMC Bioinformatics. 2023 Jan 20; 24(1):23.
Score: 0.533
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xAtlas: scalable small variant calling across heterogeneous next-generation sequencing experiments. Gigascience. 2022 12 28; 12.
Score: 0.531
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PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation. Genome Biol. 2021 09 14; 22(1):268.
Score: 0.486
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Parliament2: Accurate structural variant calling at scale. Gigascience. 2020 12 21; 9(12).
Score: 0.462
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PhaseME: Automatic rapid assessment of phasing quality and phasing improvement. Gigascience. 2020 07 01; 9(7).
Score: 0.447
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Evaluation of computational genotyping of structural variation for clinical diagnoses. Gigascience. 2019 09 01; 8(9).
Score: 0.422
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Teaser: Individualized benchmarking and optimization of read mapping results for NGS data. Genome Biol. 2015 Oct 22; 16:235.
Score: 0.323
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STRspy2.0: Unlocking the Potential of Long Reads for Forensic DNA Profiling. Int J Mol Sci. 2026 Feb 16; 27(4).
Score: 0.165
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Clair3-RNA: a deep learning-based small variant caller for long-read RNA sequencing data. Nat Commun. 2025 Dec 22; 16(1):11553.
Score: 0.163
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LorBin: efficient binning of long-read metagenomes by multiscale adaptive clustering and evaluation. Nat Commun. 2025 Oct 24; 16(1):9353.
Score: 0.161
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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: 0.155
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The GIAB genomic stratifications resource for human reference genomes. Nat Commun. 2024 10 19; 15(1):9029.
Score: 0.150
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Detection of mosaic and population-level structural variants with Sniffles2. Nat Biotechnol. 2024 Oct; 42(10):1571-1580.
Score: 0.142
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muCNV: Genotyping Structural Variants for Population-level Sequencing. Bioinformatics. 2021 08 04; 37(14):2055?2057.
Score: 0.117
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RaGOO: fast and accurate reference-guided scaffolding of draft genomes. Genome Biol. 2019 10 28; 20(1):224.
Score: 0.107
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Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel. Genet Med. 2019 09; 21(9):2135-2144.
Score: 0.102
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GenomeScope: fast reference-free genome profiling from short reads. Bioinformatics. 2017 Jul 15; 33(14):2202-2204.
Score: 0.091
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NextGenMap: fast and accurate read mapping in highly polymorphic genomes. Bioinformatics. 2013 Nov 01; 29(21):2790-1.
Score: 0.069
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When less is more: sketching with minimizers in genomics. Genome Biol. 2024 Oct 14; 25(1):270.
Score: 0.038
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StratoMod: predicting sequencing and variant calling errors with interpretable machine learning. Commun Biol. 2024 10 13; 7(1):1316.
Score: 0.038
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Characterization and visualization of tandem repeats at genome scale. Nat Biotechnol. 2024 Oct; 42(10):1606-1614.
Score: 0.036
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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: 0.032
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Searching thousands of genomes to classify somatic and novel structural variants using STIX. Nat Methods. 2022 04; 19(4):445-448.
Score: 0.032
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Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment. Gigascience. 2021 09 24; 10(9).
Score: 0.030
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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: 0.025