Novel multi-nucleotide polymorphisms in the human genome characterized by whole genome and exome sequencing.
about
Limitations of the human reference genome for personalized genomicsRevising the M235T polymorphism position for the AGT gene and reporting a modifying variant in the Brazilian population with potential cardiac and neural impact.Merging Absolute and Relative Quantitative PCR Data to Quantify STAT3 Splice Variant Transcripts.Catalog of microRNA seed polymorphisms in vertebratesComprehensive characterization of human genome variation by high coverage whole-genome sequencing of forty four CaucasiansChapter 15: disease gene prioritization.A biocompatible open-surface droplet manipulation platform for detection of multi-nucleotide polymorphism.MAC: identifying and correcting annotation for multi-nucleotide variationsCodon-level co-occurrences of germline variants and somatic mutations in cancer are rare but often lead to incorrect variant annotation and underestimated impact prediction.Are sites with multiple single nucleotide variants in cancer genomes a consequence of drivers, hypermutable sites or sequencing errors?Searching for new genetic variations in expression databases for the GABAergic and glutamatergic systems.Patterns and mutational signatures of tandem base substitutions causing human inherited disease.The Visual Colorimetric Detection of Multi-nucleotide Polymorphisms on a Pneumatic Droplet Manipulation Platform.
P2860
Q28727242-3E81532D-D725-4F4B-A3D3-2CA7E15870E2Q30416011-EDB5CA7C-ECE1-4151-98EC-7AAE03D5F687Q31138278-ADDEDA2C-EE37-4F4D-8AD2-FD1254DB3371Q34150000-A44154D5-7A64-4CDA-A89A-2417169A268BQ34663567-DCECA4B6-F8E3-4BEC-B2FB-D7AA8C972966Q34697737-97039589-0BC0-42C2-B1CA-A9C93EEFB53DQ35161884-E2768C22-BFC6-4DDD-B277-70B59AE00AFCQ35731994-5962AD82-45F0-46F0-9CA0-3325290BBCADQ36325604-204B50DD-36D1-4C14-8D3C-7013A52E79FBQ37282168-FA69322C-080E-4BC1-88BE-D27CC558968AQ43465731-E424DB20-C5C8-497A-B561-2C5A684D9950Q43584644-24FD87B7-4634-4C29-8090-372BAE79C665Q51130235-E59C59E9-BD40-4CC6-9F14-65EC2C849569
P2860
Novel multi-nucleotide polymorphisms in the human genome characterized by whole genome and exome sequencing.
description
2010 nî lūn-bûn
@nan
2010 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Novel multi-nucleotide polymor ...... e genome and exome sequencing.
@ast
Novel multi-nucleotide polymor ...... e genome and exome sequencing.
@en
Novel multi-nucleotide polymor ...... e genome and exome sequencing.
@nl
type
label
Novel multi-nucleotide polymor ...... e genome and exome sequencing.
@ast
Novel multi-nucleotide polymor ...... e genome and exome sequencing.
@en
Novel multi-nucleotide polymor ...... e genome and exome sequencing.
@nl
prefLabel
Novel multi-nucleotide polymor ...... e genome and exome sequencing.
@ast
Novel multi-nucleotide polymor ...... e genome and exome sequencing.
@en
Novel multi-nucleotide polymor ...... e genome and exome sequencing.
@nl
P2860
P356
P1476
Novel multi-nucleotide polymor ...... e genome and exome sequencing.
@en
P2093
Anil K Malhotra
Jeffrey A Rosenfeld
P2860
P304
P356
10.1093/NAR/GKQ408
P407
P50
P577
2010-05-20T00:00:00Z