<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ling X</submitter><funding>National Public Sector (AQSIQ)</funding><funding>Shenzhen Municipal Committee of Science and Technology Innovation</funding><pagination>203-6</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4510450</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>4</volume><pubmed_abstract>ABI PRISM 3100 Genetic Analyzer, a multi-color fluorescence-based DNA analysis system with 16 capillaries operating in parallel, was ideal tool both for DNA sequencing and DNA fragment analysis [1,2]. To demonstrate the effectiveness and reliability of an asymmetric PCR-Based approach (X.Y. Ling, G.M. Zhang, G. Pan, H. Long, Y.H. Cheng, C.Y. Xiang, L. Kang, F. Chen, Z.N. Chen, Preparing long probes by an asymmetric PCR-based approach for multiplex ligation-dependent probe amplification (MLPA), Anal. Biochem. (2015), http://dx.doi.org/10.1016/j.ab.2015.03.031, in press) in preparing the long MLPA probes that were generated with a M13-based method before [4], some prepared long MLPA probes were sequenced and then tested in MLPA analysis. Sequencing data shows that the long MLPA probes were i</pubmed_abstract><journal>Data in brief</journal><pubmed_title>Sequencing data and MLPA analysis data in support of the effectiveness and reliability of an asymmetric PCR-Based approach in preparing long MLPA probes.</pubmed_title><pmcid>PMC4510450</pmcid><funding_grant_id>201410014-2</funding_grant_id><funding_grant_id>JC201105190969A</funding_grant_id><pubmed_authors>Pan G</pubmed_authors><pubmed_authors>Long H</pubmed_authors><pubmed_authors>Ling X</pubmed_authors><pubmed_authors>Chen Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sequencing data and MLPA analysis data in support of the effectiveness and reliability of an asymmetric PCR-Based approach in preparing long MLPA probes.</name><description>ABI PRISM 3100 Genetic Analyzer, a multi-color fluorescence-based DNA analysis system with 16 capillaries operating in parallel, was ideal tool both for DNA sequencing and DNA fragment analysis [1,2]. To demonstrate the effectiveness and reliability of an asymmetric PCR-Based approach (X.Y. Ling, G.M. Zhang, G. Pan, H. Long, Y.H. Cheng, C.Y. Xiang, L. Kang, F. Chen, Z.N. Chen, Preparing long probes by an asymmetric PCR-based approach for multiplex ligation-dependent probe amplification (MLPA), Anal. Biochem. (2015), http://dx.doi.org/10.1016/j.ab.2015.03.031, in press) in preparing the long MLPA probes that were generated with a M13-based method before [4], some prepared long MLPA probes were sequenced and then tested in MLPA analysis. Sequencing data shows that the long MLPA probes were i</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Sep</publication><modification>2026-05-30T05:50:19.547Z</modification><creation>2019-03-27T01:55:35Z</creation></dates><accession>S-EPMC4510450</accession><cross_references><pubmed>26217790</pubmed><doi>10.1016/j.dib.2015.05.008</doi></cross_references></HashMap>