Quantitative assessment of LASSO probe assembly and long-read multiplexed cloning

被引：0
作者：
Syukri Shukor
Alfred Tamayo
Lorenzo Tosi
H. Benjamin Larman
Biju Parekkadan
机构：
[1] Massachusetts General Hospital,Center for Surgery, Innovation, and Bioengineering, Department of Surgery
[2] Harvard Medical School and the Shriners Hospitals for Children,Division of Immunology, Department of Pathology
[3] Johns Hopkins University,Department of Biomedical Engineering
[4] Harvard Stem Cell Institute,undefined
[5] Rutgers University,undefined
来源：
BMC Biotechnology | / 19卷
关键词：
Long adapter single-stranded oligonucleotides (LASSO); Genomic libraries; Multiplex PCR; Multiplex cloning;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 54 条
[1]  
Mamanova L(2010)Target-enrichment strategies for next-generation sequencing Nat Methods 7 111-118
[2]  
Coffey AJ(2005)Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay Genome Res 15 269-275
[3]  
Scott CE(2016)Molecular Inversion Probes for targeted resequencing in non-model organisms Sci Rep 6 24051-905
[4]  
Kozarewa I(2007)Connector inversion probe technology: a powerful one-primer multiplex DNA amplification system for numerous scientific applications PLoS One 2 e915-2120
[5]  
Turner EH(2007)Direct selection of human genomic loci by microarray hybridization Nat Methods 4 903-359
[6]  
Kumar A(2014)Trimmomatic: a flexible trimmer for Illumina sequence data Bioinformatics 30 2114-2079
[7]  
Hardenbol P(2012)Fast gapped-read alignment with Bowtie 2 Nat Methods 9 357-842
[8]  
Yu F(2011)Sequence-specific error profile of Illumina sequencers Nucleic Acids Res 39 e90-undefined
[9]  
Belmont J(2016)Evaluating the necessity of PCR duplicate removal from next-generation sequencing data and a comparison of approaches BMC Bioinformatics 17 239-undefined
[10]  
Mackenzie J(2009)The sequence alignment/map format and SAMtools Bioinformatics 25 2078-undefined
123456