Methy-Pipe: An Integrated Bioinformatics Pipeline for Whole Genome Bisulfite Sequencing Data Analysis
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K. Sun | P. Jiang | K. C. Chan | R. Chiu | Y. Lo | Huating Wang | Hao Sun | Fiona M. F. Lun | Andy M. Guo
[1] Peiyong Jiang,et al. Noninvasive detection of cancer-associated genome-wide hypomethylation and copy number aberrations by plasma DNA bisulfite sequencing , 2013, Proceedings of the National Academy of Sciences.
[2] Peiyong Jiang,et al. Noninvasive prenatal methylomic analysis by genomewide bisulfite sequencing of maternal plasma DNA. , 2013, Clinical chemistry.
[3] J. Viegas. Profile of Dennis Lo , 2013, Proceedings of the National Academy of Sciences.
[4] Matthew D. Schultz,et al. Global Epigenomic Reconfiguration During Mammalian Brain Development , 2013, Science.
[5] Wendy P Robinson,et al. The human placenta methylome , 2013, Proceedings of the National Academy of Sciences.
[6] T. Benoukraf,et al. GBSA: a comprehensive software for analysing whole genome bisulfite sequencing data , 2012, Nucleic acids research.
[7] B. Langmead,et al. BSmooth: from whole genome bisulfite sequencing reads to differentially methylated regions , 2012, Genome Biology.
[8] W. Sung,et al. BatMeth: improved mapper for bisulfite sequencing reads on DNA methylation , 2012, Genome Biology.
[9] Francine E. Garrett-Bakelman,et al. methylKit: a comprehensive R package for the analysis of genome-wide DNA methylation profiles , 2012, Genome Biology.
[10] Steven L Salzberg,et al. Fast gapped-read alignment with Bowtie 2 , 2012, Nature Methods.
[11] Felix Krueger,et al. Bismark: a flexible aligner and methylation caller for Bisulfite-Seq applications , 2011, Bioinform..
[12] R. Stewart,et al. Hotspots of aberrant epigenomic reprogramming in human induced pluripotent stem cells , 2011, Nature.
[13] Pao-Yang Chen,et al. BS Seeker: precise mapping for bisulfite sequencing , 2010, BMC Bioinformatics.
[14] Peter L Molloy,et al. Hypomethylation of repeated DNA sequences in cancer. , 2010, Epigenomics.
[15] Chia-Lin Wei,et al. Dynamic changes in the human methylome during differentiation. , 2010, Genome research.
[16] Lee E. Edsall,et al. Human DNA methylomes at base resolution show widespread epigenomic differences , 2009, Nature.
[17] Siu-Ming Yiu,et al. High Throughput Short Read Alignment via Bi-directional BWT , 2009, 2009 IEEE International Conference on Bioinformatics and Biomedicine.
[18] Steven J. M. Jones,et al. Circos: an information aesthetic for comparative genomics. , 2009, Genome research.
[19] Siu-Ming Yiu,et al. SOAP2: an improved ultrafast tool for short read alignment , 2009, Bioinform..
[20] Wei Li,et al. BSMAP: whole genome bisulfite sequence MAPping program , 2009, BMC Bioinformatics.
[21] Cole Trapnell,et al. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome , 2009, Genome Biology.
[22] Brad T. Sherman,et al. Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists , 2008, Nucleic acids research.
[23] R. Lister,et al. Highly Integrated Single-Base Resolution Maps of the Epigenome in Arabidopsis , 2008, Cell.
[24] S. Nelson,et al. Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning , 2008, Nature.
[25] C. Ding,et al. Systematic search for placental DNA-methylation markers on chromosome 21: toward a maternal plasma-based epigenetic test for fetal trisomy 21. , 2008, Clinical chemistry.
[26] R. Yuen,et al. Hypermethylation of RASSF1A in human and rhesus placentas. , 2007, The American journal of pathology.
[27] A. Gnirke,et al. Reduced representation bisulfite sequencing for comparative high-resolution DNA methylation analysis , 2005, Nucleic acids research.
[28] R. Yung,et al. DNA methylation and the regulation of gene transcription , 2002, Cellular and Molecular Life Sciences CMLS.
[29] Brad T. Sherman,et al. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources , 2008, Nature Protocols.