about
In Silico Analysis of the deleterious nsSNP's (missense) in the Homeobox domain of human HOXB13 gene responsible for hereditary prostate cancer.Ensembl Plants: Integrating Tools for Visualizing, Mining, and Analyzing Plant Genomic Data.Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p.Function-driven discovery of disease genes in zebrafish using an integrated genomics big data resource.Independent introductions and admixtures have contributed to adaptation of European maize and its American counterparts.QueryOR: a comprehensive web platform for genetic variant analysis and prioritizationHigh throughput sequencing reveals Drosophila suzukii responses to insecticides.Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency.Whole-Genome Resequencing Identifies the Molecular Genetic Cause for the Absence of a Gy5 Glycinin Protein in Soybean PI 603408.Genetic Characterization of a French Cohort of GNE-mutation negative inclusion body myopathy patients with exome sequencing.A Sorghum Mutant Resource as an Efficient Platform for Gene Discovery in Grasses.A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study.Functional variomics and network perturbation: connecting genotype to phenotype in cancer.Exploring genetic suppression interactions on a global scale.Characterization of potential driver mutations involved in human breast cancer by computational approaches.Recombination Rate Variation, Hitchhiking, and Demographic History Shape Deleterious Load in Poplar.Morphologic and molecular study of lung cancers associated with idiopathic pulmonary fibrosis and other pulmonary fibroses.Signatures of Selection and Interspecies Introgression in the Genome of Chinese Domestic Pigs.Novel PDE6A mutation in an Emirati patient with retinitis pigmentosa.Green-fruited Solanum habrochaites lacks fruit-specific carotenogenesis due to metabolic and structural blocks.Network-Based Identification of Adaptive Pathways in Evolved Ethanol-Tolerant Bacterial Populations.Inactivation of AMMECR1 is associated with growth, bone, and heart alterations.VarCards: an integrated genetic and clinical database for coding variants in the human genome.Benchmarking distributed data warehouse solutions for storing genomic variant information.NSD1- and NSD2-damaging mutations define a subset of laryngeal tumors with favorable prognosis.Allelic spectrum of formiminotransferase-cyclodeaminase gene variants in individuals with formiminoglutamic aciduria.Genetic and functional analysis of the RYR1 mutation p.Thr84Met revealed a susceptibility to malignant hyperthermia.Next-generation sequencing (NGS)-based identification of induced mutations in a doubly mutagenized tomato (Solanum lycopersicum) population.Myopia in Chinese families shows linkage to 10q26.13.Predicting Secretory Proteins with SignalP.History repeats itself: genomic divergence in copepods.Searching for ancient balanced polymorphisms shared between Neanderthals and Modern Humans.Impact of lower uterine segment involvement in type II endometrial cancer and the unique mutational profile of serous tumors.Exploiting the Genomic Diversity of Rice (Oryza sativa L.): SNP-Typing in 11 Early-Backcross Introgression-Breeding Populations.CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability.Comparative Genomics Approaches Accurately Predict Deleterious Variants in PlantsPopulation genomic analyses of the chocolate tree, Theobroma cacao L., provide insights into its domestication processFunctional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short statureRealizing the significance of noncoding functionality in clinical genomics
P2860
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P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh-hant
name
SIFT missense predictions for genomes.
@en
SIFT missense predictions for genomes.
@nl
type
label
SIFT missense predictions for genomes.
@en
SIFT missense predictions for genomes.
@nl
prefLabel
SIFT missense predictions for genomes.
@en
SIFT missense predictions for genomes.
@nl
P2093
P2860
P356
P1433
P1476
SIFT missense predictions for genomes.
@en
P2093
Pauline C Ng
Robert Vaser
Sim Ngak Leng
P2860
P2888
P356
10.1038/NPROT.2015.123
P577
2015-12-03T00:00:00Z