Co-Authors
This is a "connection" page, showing publications co-authored by FRITZ SEDLAZECK and HEER MEHTA.
Connection Strength
1.143
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Scalable and comprehensive mosaic variant calling using DRAGEN. medRxiv. 2026 Feb 04.
Score: 0.245
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Constellation illuminates rare disease genetics. medRxiv. 2025 Nov 10.
Score: 0.241
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Enriching for Answers in Rare Diseases. medRxiv. 2025 Oct 24.
Score: 0.241
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PTPN1-related autoinflammation is a common cause of Aicardi-Gouti?res Syndrome with reduced penetrance. medRxiv. 2026 Apr 01.
Score: 0.062
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Single cell long read whole genome sequencing reveals somatic transposon activity in human brain. Commun Biol. 2025 Nov 20; 8(1):1627.
Score: 0.060
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Population-scale Long-read Sequencing in the All of Us Research Program. medRxiv. 2025 Oct 05.
Score: 0.060
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Correction: Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair. Sci Data. 2025 Aug 08; 12(1):1385.
Score: 0.059
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Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair. Sci Data. 2025 Jul 16; 12(1):1195.
Score: 0.059
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Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair. bioRxiv. 2025 Jun 14.
Score: 0.059
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Single cell long read whole genome sequencing reveals somatic transposon activity in human brain. medRxiv. 2024 Nov 11.
Score: 0.056