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All (121)
Illumina
INFINIUM
Biotechnology Information
Thermo Fisher
Sequenom
Wellcome Trust
Multiplexion
Pyrosequencing
113 More...
 

About 686 products / 1,825 snippets / 99 images

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Bioz Stars
Nucleotide polymorphic locus (SNP) rs12979860
Thermo Fisher Scientific / Applied Biosystems  
Catalog#: NUCLEOTIDE_POLYMORPHIC_LOCUS_(SNP)_RS12979860
Techniques
TaqMan Allelic Discrimination Assay, Isolation, Gradient Centrifugation (see more)
Article Snippets
".. C and T from the single nucleotide polymorphic locus (SNP) rs12979860 near the IL28B gene were analyzed in triplicate by ABI Prism 7500 TaqMan Allelic Discrimination assay .."  (see more)
85 / 100
Bioz Stars
Nucleotide polymorphic locus (SNP) rs12979860
Thermo Fisher Scientific / Applied Biosystems  
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Catalog#: NUCLEOTIDE_POLYMORPHIC_LOCUS_(SNP)_RS12979860
Techniques
TaqMan Allelic Discrimination Assay, Isolation, Gradient Centrifugation (see more)
Article Snippets
".. C and T from the single nucleotide polymorphic locus (SNP) rs12979860 near the IL28B gene were analyzed in triplicate by ABI Prism 7500 TaqMan Allelic Discrimination assay .."  (see more)
80 / 100
Bioz Stars
Single nucleotide polymorphisms (SNP) database
Cereon Genomics LLC  
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Techniques
 
Article Snippets
"To narrow the region in which SON1 was located, the Cereon Genomics single nucleotide polymorphisms (SNP) database was used to design SNP markers between THY1 and PHYB ( Neff et .."  (see more)
95+  more images
Number of SNPs on BTA 1. Venn diagram showing number of SNPs on BTA1 in the two lower density marker panels <t>(BovineSNP50</t> and BovineHD) and in whole-genome sequence data and overlapping numbers.
MARK
SEQ
Comparative genomic analysis of Chrom-pro reveals <t>SNP,</t> Indel, and SV between assembled and reference genomes. (A) Collinear regions and variations between assembled chromosomes and reference genomes of mango. (B) The SNPs between chromosomes assembled by distinct combination of software. (C) Validation of SNPs and Indels through SGS reads mapping. SNP: single <t>nucleotide</t> polymorphism, Indel: insertion and deletion, SV: structural variation.
SOFT
Biomarker Discovery
A) Schematic representation of the AR -5′UTRs and CDS. The position of the c.-547C>T mutation and the uORF are indicated. B) A Haloplex library spanning the coding region, introns, UTRs and up and downstream sequences of the AR genomic locus was prepared from DNA of the index patients′ GF and sequenced on a MiSeq benchtop sequencer. Analysis for <t>single</t> <t>nucleotide</t> polymorphisms <t>(SNP)</t> and small insertion deletions (indels) was performed by the SureCall software (Agilent). Indicated is the mutation found in the 5′UTR of the AR . A frequency of 1 corresponds to 100% of the reads. The depth indicates the number of reads covering the indicated genomic position. C) Sanger sequencing of a male control and the index patients 1 and 2. The sequences are visualized as reverse complement strand using the Chromas Lite software and show the c.-547C>T mutation in both index patients but not in the male control. D) Sanger sequencing of blood derived DNA from both index patients as well as from the mothers of the index patients. The sequences are visualized as reverse complement strand using the Chromas Lite software and show the c.-547C>T mutation in both index patients and in the patients′ mothers in a heterozygous constellation.
MUTA
SOFT
SEQ
DER-A
(A) Whole genome <t>SNP</t> maximum likelihood phylogeny of L4.4 comprised of 236 isolates from 19 different countries, including 23 isolates from the New <t>Zealand</t> <t>Rangipo</t> and Otara clusters. A black asterisk indicates the DS6 Quebec deletion. Tips and terminal branches are coloured by global region and lineages labelled according to the nomenclature of Coll et al. . A black circle indicates the node position of the most recent common ancestor of L4.4 (rooted to H37Rv, not shown). (B) Schematic of the DS6 Quebec deletion. Genomic regions in H37Rv that are deleted by the DS6 Quebec deletion and the RD152 deletion in the Beijing/W lineage are shown.
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86 / 100
Bioz Stars
Single Nucleotide Polymorphism (SNP) Database
Biotechnology Information  
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Techniques
 
Article Snippets
".. polymorphism (rs78894077) listed in the National Center for Biotechnology Information Single Nucleotide Polymorphism (SNP) Database (dbSNP; http://ncbi.nlm.nih.gov/projects/SNP/)."  (see more)
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Bioz Stars
NCBI) single-nucleotide polymorphism (SNP) database
Biotechnology Information  
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Techniques
 
Article Snippets
"Additionally, an identified GATA6 variant was checked in National Center for Biotechnology Information (NCBI) single-nucleotide polymorphism (SNP) database ( http://ncbi.nlm.nih.gov/SNP ) to confirm the novelty. table ft1 table-wrap mode="anchored" t5 Table 1. .."  (see more)
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Bioz Stars
Proprietary single nucleotide polymorphism (SNP) database
Illumina  
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Techniques
 
Article Snippets
"In Panel 1, 96 AIMs were selected from an Illumina proprietary single nucleotide polymorphism (SNP) database to maximize the difference in allele frequencies between Caucasian and .."  (see more)
80 / 100
Bioz Stars
Single nucleotide polymorphism (SNP) database (dbSNP)
Biotechnology Information  
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Techniques
 
Article Snippets
".. average of European population data from the National Center for Biotechnology Information single nucleotide polymorphism (SNP) database (dbSNP) using the Fisher exact test."  (see more)
85 / 100
Bioz Stars
Single nucleotide polymorphisms (SNP)
5 PRIME  
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Techniques
 
Article Snippets
".. metabolically characterized individuals were screened for expression of two single nucleotide polymorphisms (SNP) in the 5-prime flanking region of GFAT."  (see more)
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Bioz Stars
Single nucleotide polymorphism (SNP)
The Jackson Laboratory  
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Techniques
 
Article Snippets
"Translational Vision Research Model 4 (Tvrm4) mice, isolated at the Jackson Laboratory in 2010, bear a single nucleotide polymorphism (SNP) in the rhodopsin gene ( rho ), resulting in an I307N mutation (substitution of isoleucine to asparagine at Position 307) .."  (see more)
80 / 100
Bioz Stars
Single-nucleotide polymorphism (SNP)
23andMe  
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Techniques
 
Article Snippets
"23andMe has provided single-nucleotide polymorphism (SNP) testing to more than 800,000 people, including about 12,000 with Parkinson disease."  (see more)
92 / 100
Bioz Stars
Single nucleotide polymorphism (SNP)-based
Thermo Fisher Scientific / Affymetrix  
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Techniques
 
Article Snippets
".. generated at Lawrence Berkeley National Laboratory using single nucleotide polymorphism (SNP)-based GeneChip Human Mapping 50K Sty arrays (Affymetrix) and compared with BAC-comparative genomic hybridization profiles .."  (see more)
91 / 100
Bioz Stars
Single nucleotide polymorphisms (SNP)
INFINIUM Inc  
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Techniques
 
Article Snippets
".. genotyping, which requires 105 to 106 features for determining genome-wide single nucleotide polymorphisms (SNP) (Infinium assay; Illumina) (70)."  (see more)
91 / 100
Bioz Stars
Single-nucleotide polymorphisms (SNP)
Illumina  
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Techniques
 
Article Snippets
".. a study of signatures of selection in Senepol using 47 K single-nucleotide polymorphisms (SNP) from Illumina's BovineSNP50 proposed a new candidate gene, Retinoic Acid induced 14 gene .."  (see more)