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Category:All HeadlinesWorld & GeopoliticsMarkets & EconomyTech & AIPoliticsSearch results for: "Low-Coverage Genome Seque" (30 stories)

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Flexible read-aware genotype imputation from sequence using biobank sized reference panels
Lead StoryNaturemarkets
Dec 13, 2025

Flexible read-aware genotype imputation from sequence using biobank sized reference panels

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5TTjJJaWVrTVlxNEpIX1l1OWZSM01PU1ZqSHY2Q0xoeTk3UG9vZVAzR2M1Mm5DeFJxSl95alJwV1lDdWM3MGIwak9zUVpFNEtGREZ1RW9HY1FNSnh6WUZJ?oc=5" target="_blank">Flexible read-aware genotype imputation from sequence using biobank sized reference panels</a>  <font color="#6f6f6f">Nature</font>

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Search Results for "Low-Coverage Genome Seque"

Updated every 3 minutes via FreeNewsApi, GNews, Currents API & Google News

29 stories displayed
Applications of low coverage sequence data to genomics of species barriers and trait variation
Cornell Universitytech

Applications of low coverage sequence data to genomics of species barriers and trait variation

<a href="https://news.google.com/rss/articles/CBMinAFBVV95cUxPdE9zYlRWUDVNd1Z4cGdlLXdOOXpiTll5VWVuZUFRUjN6X3pWSGVBUExEZFZjNV9FRllvWUVsTkl1TUItWHdZM2wtY0R1YnhoVjBmd3hmbnVqMGVJcW4xUUMyMjlveVFBR2g3RFF1ZGxDYnlrYUFGTkdIZXRsYzdkUkJXMEczMnF2UmhwSzFjVnNuU3RBb2lrLUtkMTQ?oc=5" target="_blank">Applications of low coverage sequence data to genomics of species barriers and trait variation</a>  <font color="#6f6f6f">Cornell University</font>

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Low-coverage sequencing and Wahlund effect severely bias estimates of inbreeding, heterozygosity and effective population size in North American wolves
Wiley Online Libraryworld

Low-coverage sequencing and Wahlund effect severely bias estimates of inbreeding, heterozygosity and effective population size in North American wolves

<a href="https://news.google.com/rss/articles/CBMiY0FVX3lxTE4zQ2lsSFdSR1ZGaEVWZDVOZkNwYlUyQzBPU2ozUHUzS091SzRUWnlYNkR3UzFJWEEzYWRJY2tUbmpjeXMxRnU4aE9kS0NiV1d0SnJKUGczV1RIR2MxNGdubkZtOA?oc=5" target="_blank">Low-coverage sequencing and Wahlund effect severely bias estimates of inbreeding, heterozygosity and effective population size in North American wolves</a>  <font color="#6f6f6f">Wiley Online Library</font>

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Coding-complete genome sequence of a lumpy skin disease virus (LSDV) isolate from Rajshahi, Bangladesh
ASM Journalsgeneral

Coding-complete genome sequence of a lumpy skin disease virus (LSDV) isolate from Rajshahi, Bangladesh

<a href="https://news.google.com/rss/articles/CBMiXkFVX3lxTFA3R1ZrRURBdHpPQTFQVG9PZ0JuTF84YzUwZnoyeXZMVG10VDQtcTBBWURxdmpadERyNV9vODF5Mnpfb3ZJbWhwc0FpOW1JOXVtVFpuQk1IWml6Q21qbVE?oc=5" target="_blank">Coding-complete genome sequence of a lumpy skin disease virus (LSDV) isolate from Rajshahi, Bangladesh</a>  <font color="#6f6f6f">ASM Journals</font>

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Calculating maternal polygenic risk scores from prenatal screening by cell-free DNA data
Frontiersgeneral

Calculating maternal polygenic risk scores from prenatal screening by cell-free DNA data

<a href="https://news.google.com/rss/articles/CBMijwFBVV95cUxQS2xNWjJYOHRzbkhPMzNBZDJkOXFwVllrV1F0V24zU0lwenFhTlVIWG5SaXR1SkZHWDU2cVUtVU44VTZoejdwVENOSEctQnA0TlZqa0loR1lXWFNRRlVFdERNNGJ4UklfTGZEQmFJc0ZYQUJQMExyMmgxT1lVTkQxTl9fbzVSN3pGTkVwa2FkNA?oc=5" target="_blank">Calculating maternal polygenic risk scores from prenatal screening by cell-free DNA data</a>  <font color="#6f6f6f">Frontiers</font>

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Imputation of low-coverage sequencing data from 150,119 UK Biobank genomes
Naturemarkets

Imputation of low-coverage sequencing data from 150,119 UK Biobank genomes

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBtSFdvQV9zZHJtNnhBRTIxWk15UDZPZzBsTWJIaXVnZGNORDJ5bS13ZnJlX3Rjd0t5a0JHSEdVNTloRnF6TnRKS3RfYTNhSVh6ZnZQcEgxRGNlcHFOeExJ?oc=5" target="_blank">Imputation of low-coverage sequencing data from 150,119 UK Biobank genomes</a>  <font color="#6f6f6f">Nature</font>

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Genome-wide mutational signatures in low-coverage whole genome sequencing of cell-free DNA
Naturegeneral

Genome-wide mutational signatures in low-coverage whole genome sequencing of cell-free DNA

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5mVTg2WUR2ZWZtcG9NV2h3bWlRdTM3QXFEbDZSaUsweHFjYmpEdGUzR3FHOW41NHhvb3phREVJU3lveXoydnBVNEZZVlJNQldrenZnWkxOa1BGZjBaeFBr?oc=5" target="_blank">Genome-wide mutational signatures in low-coverage whole genome sequencing of cell-free DNA</a>  <font color="#6f6f6f">Nature</font>

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The genome sequence of the outbreeding globe artichoke constructed de novo incorporating a phase-aware low-pass sequencing strategy of F1 progeny | Scientific Reports
Naturegeneral

The genome sequence of the outbreeding globe artichoke constructed de novo incorporating a phase-aware low-pass sequencing strategy of F1 progeny | Scientific Reports

<a href="https://news.google.com/rss/articles/CBMiU0FVX3lxTE1QY3FjSy0zZnVaclhHZ2lqQktwLWhSNjVJSWpkOGtsdnJiSWFYMmVmZS1zMUxGS0c3MXo2N0JST3hWVGJKSTFBeEVPSXpQeFZiZFVB?oc=5" target="_blank">The genome sequence of the outbreeding globe artichoke constructed de novo incorporating a phase-aware low-pass sequencing strategy of F1 progeny | Scientific Reports</a>  <font color="#6f6f6f">Nature</font>

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A blended genome and exome sequencing method captures genetic variation in an unbiased and cost-effective manner
Natureworld

A blended genome and exome sequencing method captures genetic variation in an unbiased and cost-effective manner

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5YWWtBSnYxSXAxdm12RlRfTUpSODBHdTZVRUFHZnpaTHVPUEUyUzVKUF9JekpaMHl3SEdydkdXWVJMSGpKSnFJWUJsSU90RmJsYl9BbmRpWVlQMFNncDRr?oc=5" target="_blank">A blended genome and exome sequencing method captures genetic variation in an unbiased and cost-effective manner</a>  <font color="#6f6f6f">Nature</font>

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Profiling of runs of homozygosity from whole-genome sequence data in Japanese biobank
Naturemarkets

Profiling of runs of homozygosity from whole-genome sequence data in Japanese biobank

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFB6dTVzckJTRHRHQnJFeW95OF9EeUc1ODRPNEVKY3J4MXBXQjdtS2pkZVRsM0tobTdZeVVFT0RyT0ZHVm5SbzFQWV9ObXU3S1FwUHRkaXRmYmt2QVprbDQw?oc=5" target="_blank">Profiling of runs of homozygosity from whole-genome sequence data in Japanese biobank</a>  <font color="#6f6f6f">Nature</font>

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Whole genome sequencing reveals high differentiation, low levels of genetic diversity and short runs of homozygosity among Swedish wels catfish
Natureworld

Whole genome sequencing reveals high differentiation, low levels of genetic diversity and short runs of homozygosity among Swedish wels catfish

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE1hTmJBV2tRZFdDOW5yMjhPM2J2RHdRRnlNSThRd0ptX1BGQzdDZDA1TnJSeC10UDkyMTB2TjdZQUo2eFJTTXVGbTRpV1k2djF2TjFfUmY5YUN4RElLWVZR?oc=5" target="_blank">Whole genome sequencing reveals high differentiation, low levels of genetic diversity and short runs of homozygosity among Swedish wels catfish</a>  <font color="#6f6f6f">Nature</font>

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Toward genomic prediction from whole-genome sequence data: impact of sequencing design on genotype imputation and accuracy of predictions
Naturegeneral

Toward genomic prediction from whole-genome sequence data: impact of sequencing design on genotype imputation and accuracy of predictions

<a href="https://news.google.com/rss/articles/CBMiU0FVX3lxTE9TT1drRUdneGp0Y0c0cVBVWDg5OW9xejNoZDUyWkFyRy1pMUhQd3h4TlktR280dTljNDRYUGZYMWVaU3dXVFl0QUozdFRHbEtuNXdJ?oc=5" target="_blank">Toward genomic prediction from whole-genome sequence data: impact of sequencing design on genotype imputation and accuracy of predictions</a>  <font color="#6f6f6f">Nature</font>

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Novel metrics to measure coverage in whole exome sequencing datasets reveal local and global non-uniformity
Natureworld

Novel metrics to measure coverage in whole exome sequencing datasets reveal local and global non-uniformity

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE04a2VLdzJMdmRQQ01yNThQX2h1OGkxTGlCc3lDczQzWWE5M05UQnAwaGpuOW1rV1pnSDQzbURFYWd2MjBQS2FqU0xoVVBYTVAwbzkxVU9tdlowRGtlYjFF?oc=5" target="_blank">Novel metrics to measure coverage in whole exome sequencing datasets reveal local and global non-uniformity</a>  <font color="#6f6f6f">Nature</font>

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A high-throughput skim-sequencing approach for genotyping, dosage estimation and identifying translocations
Naturegeneral

A high-throughput skim-sequencing approach for genotyping, dosage estimation and identifying translocations

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE83NTV2MXc4LXBkRnhHVjQ4bFRhcFN3VjM2dVpJb2VYWjdtakhOZG1HYzBlMXJXZk44UUpzU19ySHBSTlItWGs0RzNkVnNXc3QyVmFvTTNIaHYySTZLRmR3?oc=5" target="_blank">A high-throughput skim-sequencing approach for genotyping, dosage estimation and identifying translocations</a>  <font color="#6f6f6f">Nature</font>

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Next generation sequencing has lower sequence coverage and poorer SNP-detection capability in the regulatory regions
Naturegeneral

Next generation sequencing has lower sequence coverage and poorer SNP-detection capability in the regulatory regions

<a href="https://news.google.com/rss/articles/CBMiU0FVX3lxTE1mWDFxQkhzMl93M0xuQWJsREI0bWVZVmVLbnptVlV3NnBDS0NwZmpjaHpCRDNfazRjcmNQUVdPVjJhRG5EYjVvSl9mVzFCckdyMVY0?oc=5" target="_blank">Next generation sequencing has lower sequence coverage and poorer SNP-detection capability in the regulatory regions</a>  <font color="#6f6f6f">Nature</font>

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High confidence copy number variants identified in Holstein dairy cattle from whole genome sequence and genotype array data
Naturetech

High confidence copy number variants identified in Holstein dairy cattle from whole genome sequence and genotype array data

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5UZmRYQmtpZmtfcmRGODRKYTR0dXE3M2RHVC1nZnhLM0wzb2VRS1VBWllZS0YxNmRJc01vU3M2bmhWa2xDaHZ4UTBHbXpZY0ttZE9JM3Z4cHZPN19YZ21n?oc=5" target="_blank">High confidence copy number variants identified in Holstein dairy cattle from whole genome sequence and genotype array data</a>  <font color="#6f6f6f">Nature</font>

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Genome sequence analysis provides evidence that a boreal crustacean colonised Svalbard well before the ongoing Atlantification of the Arctic | Heredity
Naturegeneral

Genome sequence analysis provides evidence that a boreal crustacean colonised Svalbard well before the ongoing Atlantification of the Arctic | Heredity

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5PaUsweFYxLWY3X1d0d1BaT01NWEpPMTJ3Q1hKekpoNzVKeDJ2RENHVDJ4S0dSZy1DSWNVUFU2clN0QkQ2LVM5Vmx0WjR2OFROM3hERUZNQ1U4MkwtUFJV?oc=5" target="_blank">Genome sequence analysis provides evidence that a boreal crustacean colonised Svalbard well before the ongoing Atlantification of the Arctic | Heredity</a>  <font color="#6f6f6f">Nature</font>

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Utility of long-read sequencing for All of Us
Naturegeneral

Utility of long-read sequencing for All of Us

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBnVF9wUFFibFBNT3hoOEl1ZlNBUjFPbnBOdVdBcHFSM3g0Y1gzOHNoMUo1Zmd0SGVxblVTWHNYWm9wSWRhNzBqbnRSdFZHNFp1RFdERGRBSVBjd25IMVVF?oc=5" target="_blank">Utility of long-read sequencing for All of Us</a>  <font color="#6f6f6f">Nature</font>

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Sequence diversity lost in early pregnancy
Naturegeneral

Sequence diversity lost in early pregnancy

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBYQjdueC1od0tOc3FVaVNCeWUwR3hTZzROelZscnlJSk9kNnJYOWh2ZXZvTFNuRWZ0RFUxb3RMS0lBdjJjTzlKbzJzd2VKOHRneHNHSmNDV0dPdmJWcDJr?oc=5" target="_blank">Sequence diversity lost in early pregnancy</a>  <font color="#6f6f6f">Nature</font>

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Assessing the efficacy of target adaptive sampling long-read sequencing through hereditary cancer patient genomes
Naturegeneral

Assessing the efficacy of target adaptive sampling long-read sequencing through hereditary cancer patient genomes

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5CdnBpa2xyNEx6Tzd3aWtfajRjWFgzVmVrenBsWGtXOXZndDNtenNNalF4a0YyUnZhUkJnTVFRQ1dPTHVLeTIwRVY2d015VVAxU0FSbERKSXFBZm54UWFV?oc=5" target="_blank">Assessing the efficacy of target adaptive sampling long-read sequencing through hereditary cancer patient genomes</a>  <font color="#6f6f6f">Nature</font>

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Information recovery from low coverage whole-genome bisulfite sequencing
Naturegeneral

Information recovery from low coverage whole-genome bisulfite sequencing

<a href="https://news.google.com/rss/articles/CBMiVkFVX3lxTE12bjM0elNlQTNhdFk0b3U0VUNyQnFKOEd2OUlKN0RCcnNGTUNtMUxuTlk2cVJlUnFaZnEzMTkwTjlwamQ5RmFPV3ZYX3MzcXZMM2NQRHVn?oc=5" target="_blank">Information recovery from low coverage whole-genome bisulfite sequencing</a>  <font color="#6f6f6f">Nature</font>

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Disease-associated genes routinely missed in some genetic studies
The Pennsylvania State Universitygeneral

Disease-associated genes routinely missed in some genetic studies

<a href="https://news.google.com/rss/articles/CBMipAFBVV95cUxPSFZIRlVUaTVJbFlNQzJBUlZlM1JtNk9NWXZ6R2VTdTItMkdlOF9xTzFmbGtWVkJkUDhiTGxYQlVWUFFSbUFtRkJ2MGg0dzdhVDZMYjh4ZGN3X2NiZGdQay1mdENsLW1PQ2tTcWRiM3ZrNU5IZW9DZ0dGMUVCYWpJQ1VibHExZHhxNmwyVFRiTDBJZU9ZNEktR2g2ZVhtdzBiRl9sOA?oc=5" target="_blank">Disease-associated genes routinely missed in some genetic studies</a>  <font color="#6f6f6f">The Pennsylvania State University</font>

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OBGYN
Wiley & Sonsgeneral

OBGYN

<a href="https://news.google.com/rss/articles/CBMib0FVX3lxTE12a1VHaHFWOElpQVFhSGs2aHh4d3lZR3czSkw3YmxSRkRKbkNUVUJsbmJXa1lHbFJ1VUlvZkcwclVoSlIzNG5xU3Vsd0tySDNzU3VUZk9JT2c3YVBjU2paTEZBUFVIM0l5d1R5VEwtZw?oc=5" target="_blank">OBGYN</a>  <font color="#6f6f6f">Wiley & Sons</font>

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A benchmarking of human mitochondrial DNA haplogroup classifiers from whole-genome and whole-exome sequence data
Naturegeneral

A benchmarking of human mitochondrial DNA haplogroup classifiers from whole-genome and whole-exome sequence data

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE1ZRmp0aEJpdHJSNjJEcXByeWpnYlhHSEhyUzlOTkNJeldtN1JRd0tGamVtWGxKQ0JTTzNxeVRVaTlEZWVkckVMWHVpQ0VPd1FneW5MV2QwVE4zQWczSGtj?oc=5" target="_blank">A benchmarking of human mitochondrial DNA haplogroup classifiers from whole-genome and whole-exome sequence data</a>  <font color="#6f6f6f">Nature</font>

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TOFU-MAaPO: fast, scalable and reproducible analysis of large metagenome sequence data from the Sequence Read Archive
Naturegeneral

TOFU-MAaPO: fast, scalable and reproducible analysis of large metagenome sequence data from the Sequence Read Archive

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE95X2RIeG9uaGFiMG43b2FBbTJSeUtHTzRDMWZWNnNDZTBFZVUzTjlpcTREcUFZWTgzYzRzREZnM3A3T2d6bjBCelI1LUNsZU04SzA1SHpMaEhaYTdfVmN3?oc=5" target="_blank">TOFU-MAaPO: fast, scalable and reproducible analysis of large metagenome sequence data from the Sequence Read Archive</a>  <font color="#6f6f6f">Nature</font>

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Earliest modern human genomes constrain timing of Neanderthal admixture
Naturetech

Earliest modern human genomes constrain timing of Neanderthal admixture

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5VcFFYMHQyWUVYVHJIM2s5ajlZWklxZlVLaUt1VzJhdk1zQlFQcTV1alZoVDRCLWNlNW1sT0tfTEhhOEs1eEpOTVFfMFpSVzhvNG04UVN0MXphMVVBRjZJ?oc=5" target="_blank">Earliest modern human genomes constrain timing of Neanderthal admixture</a>  <font color="#6f6f6f">Nature</font>

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A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica
Naturegeneral

A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE1pLXdTWkhCUHFBRlNtUHNFT204Sm9SSl9NRk1YSThoLUE1S2piTXF3UVN1dVBjajFqVTVpZG14SjVSQ19LSWFrMWNpZTY5bnFFNWFTeEVvLW5xNExMd2JJ?oc=5" target="_blank">A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica</a>  <font color="#6f6f6f">Nature</font>

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Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
Naturegeneral

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

<a href="https://news.google.com/rss/articles/CBMiVEFVX3lxTFA3SVltRVdEQnNzOXdOV0FBRDVLR2NSTjVwVDBFSHo4eWs0R2RVcndmdUxETkM4bV9JUm12SU5qeDBXcWt2QXFyWS1MQl83WDRRcGlQbQ?oc=5" target="_blank">Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel</a>  <font color="#6f6f6f">Nature</font>

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Predicting RNA-seq coverage from DNA sequence as a unifying model of gene regulation
Natureworld

Predicting RNA-seq coverage from DNA sequence as a unifying model of gene regulation

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9jUmpvdE81eHhpNDduRnNEVVFBYks5ZF9pRGJwRnQxNi15dzFMaDRob1pJMGMtMXdGZUI4Qm90Z0ljMjEwcUN6U3RESjZQMGtxa25JV0RBWGF1QjN3SVQw?oc=5" target="_blank">Predicting RNA-seq coverage from DNA sequence as a unifying model of gene regulation</a>  <font color="#6f6f6f">Nature</font>

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Longshot enables accurate variant calling in diploid genomes from single-molecule long read sequencing
Naturegeneral

Longshot enables accurate variant calling in diploid genomes from single-molecule long read sequencing

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9mQTBNcWZYVlBQeWJfZTd4RDdFQUVNbHhIQjllOUNsVEhSME0wd19xTGFzdlNXU3FYSkptdXNHWnJCSDJ0SHRZVktXd3ZGcExwRjZuekJyTEdCZlBVbmV3?oc=5" target="_blank">Longshot enables accurate variant calling in diploid genomes from single-molecule long read sequencing</a>  <font color="#6f6f6f">Nature</font>

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"Low-Coverage Genome Seque" — Live Google News Trends & Headlines