pubmed-article:19309528 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19309528 | lifeskim:mentions | umls-concept:C0012892 | lld:lifeskim |
pubmed-article:19309528 | lifeskim:mentions | umls-concept:C0184511 | lld:lifeskim |
pubmed-article:19309528 | lifeskim:mentions | umls-concept:C0039476 | lld:lifeskim |
pubmed-article:19309528 | lifeskim:mentions | umls-concept:C0017429 | lld:lifeskim |
pubmed-article:19309528 | lifeskim:mentions | umls-concept:C0205369 | lld:lifeskim |
pubmed-article:19309528 | lifeskim:mentions | umls-concept:C1521871 | lld:lifeskim |
pubmed-article:19309528 | lifeskim:mentions | umls-concept:C0205250 | lld:lifeskim |
pubmed-article:19309528 | lifeskim:mentions | umls-concept:C0205197 | lld:lifeskim |
pubmed-article:19309528 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
pubmed-article:19309528 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
pubmed-article:19309528 | lifeskim:mentions | umls-concept:C0206415 | lld:lifeskim |
pubmed-article:19309528 | pubmed:dateCreated | 2009-4-1 | lld:pubmed |
pubmed-article:19309528 | pubmed:abstractText | Whole genome amplification (WGA) is a practical solution to eliminate molecular analysis limitations associated with genomic DNA (gDNA) quantity. Different methods have been developed to amplify the whole genome, including primer extension preamplification (PEP), degenerate oligonucleotide primed PCR (DOP-PCR), and multiple displacement amplification (MDA). Each of these methods has its own merits and limitations. | lld:pubmed |
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pubmed-article:19309528 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19309528 | pubmed:language | eng | lld:pubmed |
pubmed-article:19309528 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19309528 | pubmed:status | PubMed-not-MEDLINE | lld:pubmed |
pubmed-article:19309528 | pubmed:issn | 1756-0500 | lld:pubmed |
pubmed-article:19309528 | pubmed:author | pubmed-author:MeyerBrian... | lld:pubmed |
pubmed-article:19309528 | pubmed:author | pubmed-author:AlsmadiOsamaO | lld:pubmed |
pubmed-article:19309528 | pubmed:author | pubmed-author:AlkayalFadiF | lld:pubmed |
pubmed-article:19309528 | pubmed:author | pubmed-author:MoniesDorotaD | lld:pubmed |
pubmed-article:19309528 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:19309528 | pubmed:volume | 2 | lld:pubmed |
pubmed-article:19309528 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19309528 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19309528 | pubmed:pagination | 48 | lld:pubmed |
pubmed-article:19309528 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:19309528 | pubmed:articleTitle | Specific and complete human genome amplification with improved yield achieved by phi29 DNA polymerase and a novel primer at elevated temperature. | lld:pubmed |
pubmed-article:19309528 | pubmed:affiliation | Genetics Department, Research Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. oalsmadi@kfshrc.edu.sa | lld:pubmed |
pubmed-article:19309528 | pubmed:publicationType | Journal Article | lld:pubmed |