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Category:All HeadlinesWorld & GeopoliticsMarkets & EconomyTech & AIPoliticsSearch results for: "Sequence Variations in PC" (30 stories)

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Genetic architecture and clinical features of Tourette syndrome in a child and adolescent cohort: an explorative clinical exome-based study
Lead StoryFrontiersgeneral
Jan 19

Genetic architecture and clinical features of Tourette syndrome in a child and adolescent cohort: an explorative clinical exome-based study

<a href="https://news.google.com/rss/articles/CBMikgFBVV95cUxOR3Q0anc2MlhudGhoT2NHQ1ZFcmJLU0NrN3FZVGphXzNHUk9BYVdrbEFfd3dLMEpqM19SbmhpczNGY0pQektFUkxFOUstNE1VX1hRR2hpQ2FKd2Y2aEUweDAtbjJ5cnowbGtYOWVGUjdtOHpWYVh0Mkd0cldsMWJqUFJBUko4Rm1LQThxalJiMUpLUQ?oc=5" target="_blank">Genetic architecture and clinical features of Tourette syndrome in a child and adolescent cohort: an explorative clinical exome-based study</a>  <font color="#6f6f6f">Frontiers</font>

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Search Results for "Sequence Variations in PC"

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

29 stories displayed
Genotyping sequence-resolved copy number variation using pangenomes reveals paralog-specific global diversity and expression divergence of duplicated genes
Naturegeneral

Genotyping sequence-resolved copy number variation using pangenomes reveals paralog-specific global diversity and expression divergence of duplicated genes

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9wakVKdWVHUHhWaUlpTURpYXQ0YUFQdG45NVByT3RNOVo5TWJmYzF2MThHZHNDSk5GUkdGRmNUYWM0WmhkTzNtUUJxbVpEQWFvanZzTTNLa0JuTHZ0X1JN?oc=5" target="_blank">Genotyping sequence-resolved copy number variation using pangenomes reveals paralog-specific global diversity and expression divergence of duplicated genes</a>  <font color="#6f6f6f">Nature</font>

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Sequence variations in the public human genome data reflect a bottlenecked population history
PNASgeneral

Sequence variations in the public human genome data reflect a bottlenecked population history

<a href="https://news.google.com/rss/articles/CBMiW0FVX3lxTE9MSHRsM3lNdWxYRU5ZTWtHMy1yTlh2OWRqenMwMDFLdjAwNjJvT05ORmFFWTN6d2RuemhDR2FIbnhvaktSWWQ2ajZCWFJ2Ym9Tb2dPeXBrWk92Zm8?oc=5" target="_blank">Sequence variations in the public human genome data reflect a bottlenecked population history</a>  <font color="#6f6f6f">PNAS</font>

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First complete sequence of a human genome
National Institutes of Health (NIH) | (.gov)general

First complete sequence of a human genome

<a href="https://news.google.com/rss/articles/CBMikwFBVV95cUxPVUV5ZURjYjlHMVN0NjBraC1qd1lrajUxX1FqQTlnOFhhZ1ZmTmE4MGJNTk9jcXg4V0lQXzZXaHNUR1dxRThrY3ZhbjBCeThtLThMTHVHNFVyQzFyMjN4SDg0NVEwZ0p2NjNfTVUtZURRNUQ2WEdRZ2VaUzhLN2tEbVY2QUZ6UVF5S19XVkZsclphT3c?oc=5" target="_blank">First complete sequence of a human genome</a>  <font color="#6f6f6f">National Institutes of Health (NIH) | (.gov)</font>

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Germline sequence variation in cancer genes in Rwandan breast and prostate cancer cases | npj Genomic Medicine
Naturegeneral

Germline sequence variation in cancer genes in Rwandan breast and prostate cancer cases | npj Genomic Medicine

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5IS2tLYnd6cnJkQU5mYnpKRUZLS1d1dXZJQXI5UjBiMi14ZWhNM3d1Z3VmMkwweTJKc3FNQjByQjlEZWVVZWJ3YUFFRVRVU2hSLWRqZmdCNU1qYms1eTJF?oc=5" target="_blank">Germline sequence variation in cancer genes in Rwandan breast and prostate cancer cases | npj Genomic Medicine</a>  <font color="#6f6f6f">Nature</font>

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Computational approaches for predicting variant impact: An overview from resources, principles to applications
Frontiersgeneral

Computational approaches for predicting variant impact: An overview from resources, principles to applications

<a href="https://news.google.com/rss/articles/CBMijgFBVV95cUxPNkFmWG4tNUtQN3prRFd4N2JUbGhQNWZiRTNpQ0pMQlE4UTR2YndOMnJlbWw3SjR4RTdnZ3BHTFRQNHoxckZHZ2hWMW91V0xOenp1VnllYXhKNjJxTDJQXzhRZHNyZ24yZnRWNy1CQ2I0RDRhT1lTQUYwRFNqM0ZtQjdSeVVNYlVJUndUQTBR?oc=5" target="_blank">Computational approaches for predicting variant impact: An overview from resources, principles to applications</a>  <font color="#6f6f6f">Frontiers</font>

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Accounting for small variations in the tracrRNA sequence improves sgRNA activity predictions for CRISPR screening
Natureworld

Accounting for small variations in the tracrRNA sequence improves sgRNA activity predictions for CRISPR screening

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5fSEYtM01VZXpJWmNmMHZ6Ri1DUGlncEh2YmEtTHcySXBhVzY4cHM5V3ptMVBNYUwtT0x1VHhYRGZodE8xMzFJbWhtLWhIcFNJRk02QVY2Ykl3S1hpR193?oc=5" target="_blank">Accounting for small variations in the tracrRNA sequence improves sgRNA activity predictions for CRISPR screening</a>  <font color="#6f6f6f">Nature</font>

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ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007
Naturegeneral

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007

<a href="https://news.google.com/rss/articles/CBMiU0FVX3lxTFBOcjBUc3BKTGtNTGtiaVZNTERuMUlkZzlMdnRDTnF1YzRNNjFxNnZJR3ppRWtucW1GU195R3VSeXl2SUxHdDRUQXVuN05rbHR2OE5N?oc=5" target="_blank">ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007</a>  <font color="#6f6f6f">Nature</font>

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A sequence-based global map of regulatory activity for deciphering human genetics
Naturegeneral

A sequence-based global map of regulatory activity for deciphering human genetics

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5qX0o2d1V0ME50THBPNnNmN25TTTluOHJsaEk4am01dlBReVFkT0hiRGpLdkFvNVBhWDZLV3BfQzRiMDZWNzVnNUQzMm9EQlFQYzFnbHY5VDRNX290NktB?oc=5" target="_blank">A sequence-based global map of regulatory activity for deciphering human genetics</a>  <font color="#6f6f6f">Nature</font>

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Nanopore sequencing identifies parent-of-origin specific age-associated methylation changes at imprinted loci in the human genome
Naturegeneral

Nanopore sequencing identifies parent-of-origin specific age-associated methylation changes at imprinted loci in the human genome

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE05Zm9yMktEdXBJRlZXanZIOWRlMjl2QWZjMWpqVE10bk5QTUpLLU5IaEs0NlBZdUdxTUNobDJZVmJTczNVUFFPTlRwYURtREhPclM1UTZxamFaQmVCbWlR?oc=5" target="_blank">Nanopore sequencing identifies parent-of-origin specific age-associated methylation changes at imprinted loci in the human genome</a>  <font color="#6f6f6f">Nature</font>

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Graph-based pan-genome reveals structural and sequence variations related to agronomic traits and domestication in cucumber
Naturetech

Graph-based pan-genome reveals structural and sequence variations related to agronomic traits and domestication in cucumber

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE1CZV9Ka1l5aUdwMTJXMkZnaVNTQW1HSk93bUgwQjZvSW1SQXZ6ZnZVT1hMYTJhbXoxWUxGV3RvRXRST0d5c2M3aGFQYjNIRzF3amZmRFZscThqcXE0WU00?oc=5" target="_blank">Graph-based pan-genome reveals structural and sequence variations related to agronomic traits and domestication in cucumber</a>  <font color="#6f6f6f">Nature</font>

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Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing
Naturegeneral

Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE42SXFsZmtMYm1BZHZjQW93RGp5MkxzSnhQUVFWcmQxTGpoVnU0TUlUTDBEZ3dBVE1FZlNrM0tINnk2V0ZleWZGTXA3eldSV1hNWWZWX1RVQjQ1SVE5M2lN?oc=5" target="_blank">Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing</a>  <font color="#6f6f6f">Nature</font>

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Identification of rare sequence variation underlying heritable pulmonary arterial hypertension
Natureworld

Identification of rare sequence variation underlying heritable pulmonary arterial hypertension

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE55dHpHN1d2OV9zR2t3WF95TFdkTzhRNnVycEdITVExWU9HLUs0alZIZ19nbktxNlFqNWdtUGhobTFHekx6cHpWZHY2QmJtejhHaXlZWlpoRy11anc3Nm9V?oc=5" target="_blank">Identification of rare sequence variation underlying heritable pulmonary arterial hypertension</a>  <font color="#6f6f6f">Nature</font>

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A chickpea genetic variation map based on the sequencing of 3,366 genomes
Naturegeneral

A chickpea genetic variation map based on the sequencing of 3,366 genomes

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFAyRkVpeDRzZzYydmJxNUtGcDhUQklYRE1jd21td1pjcEhYZE5uc2FjQ1Z5SkdqcHpLcXpCU1lmYWlNWjNEcm9wM1ZrRHVLRHkxQXNJU0k1RER2MGpSQVZV?oc=5" target="_blank">A chickpea genetic variation map based on the sequencing of 3,366 genomes</a>  <font color="#6f6f6f">Nature</font>

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Whole-genome sequencing analysis identifies rare, large-effect noncoding variants and regulatory regions associated with circulating protein levels
Naturegeneral

Whole-genome sequencing analysis identifies rare, large-effect noncoding variants and regulatory regions associated with circulating protein levels

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE1WZ0pRUEFhdHpFbUt6N3JCLVVlblZxZVA2MTREeXAzb2RoY3ltdFhxLU1pNGFfcVVMX0w0WEY4ZVNMRWdsMFlxa18wYmFValdscEdLN2ZXWWV1RVZIQThz?oc=5" target="_blank">Whole-genome sequencing analysis identifies rare, large-effect noncoding variants and regulatory regions associated with circulating protein levels</a>  <font color="#6f6f6f">Nature</font>

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Genotyping, sequencing and analysis of 140,000 adults from Mexico City
Naturegeneral

Genotyping, sequencing and analysis of 140,000 adults from Mexico City

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE92ZUgzMXQwZDI1WHp0ckVIMXQyRXFqTktRT2dOczVxekVkVEFsYU9udHhoNkRudXVwblZwVFZWdHI5c2QzVVBfOUJ6MXFKQnhaMWhRQVBnZUltaTRSdWhJ?oc=5" target="_blank">Genotyping, sequencing and analysis of 140,000 adults from Mexico City</a>  <font color="#6f6f6f">Nature</font>

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A small molecule stabilizer rescues the surface expression of nearly all missense variants in a GPCR
Naturegeneral

A small molecule stabilizer rescues the surface expression of nearly all missense variants in a GPCR

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5oRG1GVDJsTWNTTWZRX2hBM0tjd2FQelB0eTRROS14SWVhM1ByNEltZTdraVg4SllKclEzTEh3b2lXdUduYnlDeWNuNUpzbm1SVzB0N2xVUTZKSnFKUHQw?oc=5" target="_blank">A small molecule stabilizer rescues the surface expression of nearly all missense variants in a GPCR</a>  <font color="#6f6f6f">Nature</font>

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Estimation and mapping of the missing heritability of human phenotypes
Naturegeneral

Estimation and mapping of the missing heritability of human phenotypes

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE44amxiREJUbXB4cWZ4Z0Ruc2hTZHhSUmFHMEdZbV9MRGtrbDFwTEFoSEszajBMVm95LThaTldNcVc0Uk5tYUpZZ0NmdDNCdlI3dXlJYlpjLVBzTlVKRnpB?oc=5" target="_blank">Estimation and mapping of the missing heritability of human phenotypes</a>  <font color="#6f6f6f">Nature</font>

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Systematically developing a registry of splice-site creating variants utilizing massive publicly available transcriptome sequence data
Naturetech

Systematically developing a registry of splice-site creating variants utilizing massive publicly available transcriptome sequence data

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBHT2lJamd6Y0JVZzEwOWJDZUNLdHVia014QkRpSUtoUHg0aE45dUF5Q0xldmxtdEZNOGtaNmdGY0JTdWsyLUtmMmN2TUgtbzVHR1dEdFRKOWdKckJXRE53?oc=5" target="_blank">Systematically developing a registry of splice-site creating variants utilizing massive publicly available transcriptome sequence data</a>  <font color="#6f6f6f">Nature</font>

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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Naturegeneral

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBVVC1FaDdDclR0RnVPQ21qTExHdjBNQkp3ZDRyUTB5bjhsNnl5aDNYV2EwTEpTd3RIN0xDSE81bVBOb0dPN1lfeGdCVFF4MG4wUlplbERudUlmcUItaVhv?oc=5" target="_blank">Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program</a>  <font color="#6f6f6f">Nature</font>

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Structural implications of BK polyomavirus sequence variations in the major viral capsid protein Vp1 and large T-antigen: a computational study
ASM Journalsgeneral

Structural implications of BK polyomavirus sequence variations in the major viral capsid protein Vp1 and large T-antigen: a computational study

<a href="https://news.google.com/rss/articles/CBMiY0FVX3lxTFBYU0tqaEhRWHh2b0ZyQVhRNTc4c2dpVFlWcmgwS2dVM0NtdEJpZ1ZrNWRqNjFGeU1EdFJaYm10TUtVbnZuZ0tqOW11UDlQMlFmUlgzY1hUenprQWFmUHdsZUU2MA?oc=5" target="_blank">Structural implications of BK polyomavirus sequence variations in the major viral capsid protein Vp1 and large T-antigen: a computational study</a>  <font color="#6f6f6f">ASM Journals</font>

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Whole-genome sequencing analyses suggest novel genetic factors associated with Alzheimer’s disease and a cumulative effects model for risk liability
Naturegeneral

Whole-genome sequencing analyses suggest novel genetic factors associated with Alzheimer’s disease and a cumulative effects model for risk liability

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9GclU4Ulo1ci1wTXVGejVXYS13QjE3MDFFd1JPRFVzSEtxYUdoWkJjeEE5cTlZREdOM0lqUkFRbWcyTGUzWW9qSVlNNnltODVLRlFjeGo5ejk0UlVaQjE0?oc=5" target="_blank">Whole-genome sequencing analyses suggest novel genetic factors associated with Alzheimer’s disease and a cumulative effects model for risk liability</a>  <font color="#6f6f6f">Nature</font>

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Cancer-Type Specific Prognostic Impact of Concurrent TP53 and KRAS Alterations: A Multi-Cohort Genomic Analysis
medRxivgeneral

Cancer-Type Specific Prognostic Impact of Concurrent TP53 and KRAS Alterations: A Multi-Cohort Genomic Analysis

<a href="https://news.google.com/rss/articles/CBMifEFVX3lxTE5BTWg0X21zMVB3N2JobURvOTVrTjZpM2tpWmx0X0IzZm5yajdOX1JpX2tQc3YyTk9BeVVjMXYzRVNJUkNWQzN2MFBaQXMyS3F5TXpRaHVuVC1yRmtQYUpFWFZCSk03c3ZMdDhPcDFIbGptN2x1Q2tCcV9ST1U?oc=5" target="_blank">Cancer-Type Specific Prognostic Impact of Concurrent TP53 and KRAS Alterations: A Multi-Cohort Genomic Analysis</a>  <font color="#6f6f6f">medRxiv</font>

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Inferring the molecular and phenotypic impact of amino acid variants with MutPred2
Naturegeneral

Inferring the molecular and phenotypic impact of amino acid variants with MutPred2

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5TS0taS09nczY3QkNhQTQyZW9aaERXWjU1Ulh3YUc3SzEteFFzMm44YjlEZDd3clEtREk5YUxGY213bVFTTUdlNG5TSnZkczI0M0lVZkN2eDZJWmN2NFBF?oc=5" target="_blank">Inferring the molecular and phenotypic impact of amino acid variants with MutPred2</a>  <font color="#6f6f6f">Nature</font>

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Multimodal single cell sequencing implicates chromatin accessibility and genetic background in diabetic kidney disease progression
Natureworld

Multimodal single cell sequencing implicates chromatin accessibility and genetic background in diabetic kidney disease progression

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5JSnFXTzJ4VlQ3b2VobTVWZlJydW5mV2FSd181NlQtWDB4RENOb2dvQlRubXVocXdDZWxINFYwZ2tPamxFeXdaWjRreEVlcjFpZWdPR09CdmNiSjVqWlRr?oc=5" target="_blank">Multimodal single cell sequencing implicates chromatin accessibility and genetic background in diabetic kidney disease progression</a>  <font color="#6f6f6f">Nature</font>

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Multimodal scanning of genetic variants with base and prime editing
Naturegeneral

Multimodal scanning of genetic variants with base and prime editing

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9JZnQyRUpUbXA4QU1qekpvUzY2Z1VKMW1ncVBHSlR3aFY5X3JRRE00Nl96V0dWWkJBckd5X05tcmtSZDJtS09MaWZKcTNXVjU4dUFWTFlfYU9XSm5kdGlB?oc=5" target="_blank">Multimodal scanning of genetic variants with base and prime editing</a>  <font color="#6f6f6f">Nature</font>

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Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation | Molecular Psychiatry
Natureworld

Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation | Molecular Psychiatry

<a href="https://news.google.com/rss/articles/CBMiXkFVX3lxTE43QVc4MzN4cW03Z29NRmVxZXpkbjRmR1RIQ2ZSdUtQSGRhNEdqWkVXUDl5R0hRMTFyYjk0MC1zZWp3ckpKT3pZdThqTHhiM1RZSVJQTnhNZkl5ejRJWFE?oc=5" target="_blank">Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation | Molecular Psychiatry</a>  <font color="#6f6f6f">Nature</font>

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Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese
Naturetech

Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese

<a href="https://news.google.com/rss/articles/CBMiVkFVX3lxTE9mWl83T0NTWjg0VEdtQXMtTEdVZWVPNndXVWxXNlFVZW8wVWc1bUpJWWN1VmZqbDhuQjNuU3cweGt5ekM3ZFNNZTBwa25OZVJaaHdvSS1R?oc=5" target="_blank">Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese</a>  <font color="#6f6f6f">Nature</font>

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Large-scale whole-exome sequencing analyses identified protein-coding variants associated with immune-mediated diseases in 350,770 adults
Natureworld

Large-scale whole-exome sequencing analyses identified protein-coding variants associated with immune-mediated diseases in 350,770 adults

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE14UXdXSm1yZko5amdLZlV6SkhfQWhYd1VUX2VQRVZoa1JCOVJyOWtzWnpEeTFmWlgzUWdmVC1QMWdWTkRIb0d6YmNhc2FRa2Q2RWRvN05IWV84SDBYZGM4?oc=5" target="_blank">Large-scale whole-exome sequencing analyses identified protein-coding variants associated with immune-mediated diseases in 350,770 adults</a>  <font color="#6f6f6f">Nature</font>

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Genomic data in the All of Us Research Program
Naturegeneral

Genomic data in the All of Us Research Program

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9IeFBRekJGQldISTk4bS1Wbm9nTXRMRmlMcmE2ckdJRG5Kay1SemY1enZnM0RyNW1xQmVOR0tJUTJKN2tMNnhrdGZvRHBwOHEzSjFQM3dKaXp3Mk44UUtB?oc=5" target="_blank">Genomic data in the All of Us Research Program</a>  <font color="#6f6f6f">Nature</font>

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"Sequence Variations in PC" — Live Google News Trends & Headlines