Increasing the information content of STS-based genome maps: identifying polymorphisms in mapped STSs.
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PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencingHigh-Resolution Physical and Transcriptional Mapping of the Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy Locus on Chromosome 21q22.3 by FISHA sequence-ready BAC clone contig of a 2.2-Mb segment of human chromosome 1q24Direct genetic analysis by matrix-assisted laser desorption/ionization mass spectrometryOverlapping genomic sequences: a treasure trove of single-nucleotide polymorphismsMining for single nucleotide polymorphisms in pig genome sequence data.SPARSE LOGISTIC PRINCIPAL COMPONENTS ANALYSIS FOR BINARY DATAIntegration of DNA ligation and rolling circle amplification for the homogeneous, end-point detection of single nucleotide polymorphisms.The Human Genome Project--an overview.Deriving meaning from genomic information.The use of single nucleotide polymorphisms in the isolation of common disease genes.Human whole-genome shotgun sequencing.A local, high-density, single-nucleotide polymorphism map used to clone Caenorhabditis elegans cdf-1Single-nucleotide polymorphisms in soybeanEfficient approach to unique single-nucleotide polymorphism discovery.Expression-based genetic/physical maps of single-nucleotide polymorphisms identified by the cancer genome anatomy project.A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequenceFluorescence polarization in homogeneous nucleic acid analysis II: 5'-nuclease assayAldo-keto reductase (AKR) superfamily: genomics and annotation.Single nucleotide polymorphism array analysis of flow-sorted epithelial cells from frozen versus fixed tissues for whole genome analysis of allelic loss in breast cancerComplex SNP-based haplotypes in three human helicases: implications for cancer association studies.Methods and strategies for analyzing copy number variation using DNA microarrays.DNA base mismatch detection with bulky rhodium intercalators: synthesis and applications.Single-nucleotide polymorphism discovery by targeted DNA photocleavage.An efficient procedure for genotyping single nucleotide polymorphisms.The 10q25 neocentromere and its inactive progenitor have identical primary nucleotide sequence: further evidence for epigenetic modificationSequence diversity in 36 candidate genes for cardiovascular disorders.Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41.Comparison of the power and accuracy of biallelic and microsatellite markers in population-based gene-mapping methods.Molecular cytogenetic analysis of consistent abnormalities at 8q12-q22 in breast cancer.Population genetic implications from DNA polymorphism in random human genomic sequences.Single nucleotide polymorphism hunting in cyberspace.A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1DEco-TILLING: an inexpensive method for single nucleotide polymorphism discovery that reduces ascertainment bias
P2860
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P2860
Increasing the information content of STS-based genome maps: identifying polymorphisms in mapped STSs.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
@zh-hant
name
Increasing the information con ...... polymorphisms in mapped STSs.
@en
Increasing the information con ...... polymorphisms in mapped STSs.
@nl
type
label
Increasing the information con ...... polymorphisms in mapped STSs.
@en
Increasing the information con ...... polymorphisms in mapped STSs.
@nl
prefLabel
Increasing the information con ...... polymorphisms in mapped STSs.
@en
Increasing the information con ...... polymorphisms in mapped STSs.
@nl
P2093
P356
P1433
P1476
Increasing the information con ...... polymorphisms in mapped STSs.
@en
P2093
P304
P356
10.1006/GENO.1996.0019
P50
P577
1996-01-01T00:00:00Z