Evidence map›Paper›PMID 18611953›Full record

ArticleNucleic acids research2008

SNP-specific extraction of haplotype-resolved targeted genomic regions.

Johannes Dapprich, Deborah Ferriola, Eleni E Magira, Mark Kunkel, Dimitri Monos

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 27 citations in OpenAlex.

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  12. The human Major Histocompatibility Complex as a paradigm in genomics research.Briefings in functional genomics & proteomics · 2009
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Johannes DapprichGeneration Biotech, Lawrenceville, NJ 08648, USA. jdapprich@generationbiotech.com
Deborah Ferriola
Eleni E Magira
Mark Kunkel
Dimitri Monos
Children's Hospital of Philadelphia · USGeneration Biotech (United States) · USUniversity of Pennsylvania · US

Funding

A Rapid Method for HLA-typing by HaplotypingR44AI051036 · NIAID · GENERATION BIOTECH, LLC · PI DAPPRICH, JOHANNES · 2004 to 2006
$2.8M
A Rapid Method for HLA-typing by HaplotypingR43AI051036 · NIAID · GENERATION BIOTECH, LLC · PI DAPPRICH, JOHANNES · 2003 to 2003
$100k
Automated preparation of megabase genomic DNAR43HG004096 · NHGRI · GENERATION BIOTECH, LLC · PI DAPPRICH, JOHANNES · 2006 to 2006
$100k
NHGRI NIH HHS R43 HG004096NIAID NIH HHS R43 AI051036NIAID NIH HHS R43 AI51036NIAID NIH HHS R44 AI051036NIAID NIH HHS R44 AI51036
6 · The paper itself

Abstract

The availability of genotyping platforms for comprehensive genetic analysis of complex traits has resulted in a plethora of studies reporting the association of specific single-nucleotide polymorphisms (SNPs) with common diseases or drug responses. However, detailed genetic analysis of these associated regions that would correlate particular polymorphisms to phenotypes has lagged. This is primarily due to the lack of technologies that provide additional sequence information about genomic regions surrounding specific SNPs, preferably in haploid form. Enrichment methods for resequencing should have the specificity to provide DNA linked to SNPs of interest with sufficient quality to be used in a cost-effective and high-throughput manner. We describe a simple, automated method of targeting specific sequences of genomic DNA that can directly be used in downstream applications. The method isolates haploid chromosomal regions flanking targeted SNPs by hybridizing and enzymatically elongating oligonucleotides with biotinylated nucleotides based on their selective binding to unique sequence elements that differentiate one allele from any other differing sequence. The targeted genomic region is captured by streptavidin-coated magnetic particles and analyzed by standard genotyping, sequencing or microarray analysis. We applied this technology to determine contiguous molecular haplotypes across a approximately 150 kb genomic region of the major histocompatibility complex.

Indexed as

HaplotypesPolymorphism, Single NucleotideAllelesDNAGenomicsHistocompatibility Antigens Class IHLA-B AntigensHLA-C AntigensHumansMajor Histocompatibility ComplexMicrosatellite RepeatsDNAHistocompatibility Antigens Class IHLA-B AntigensHLA-C AntigensMHC class I-related chain A

Identifiers

PMID18611953
PMCPMC2528194
OpenAlexW1964644844

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.