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CNV-seq, a new method to detect copy number variation ...www.ncbi.nlm.nih.gov › … › BMC Bioinformatics › v.10; 2009DNA copy number variation (CNV) has been recognized as an important source of genetic variation. Array comparative genomic hybridization (aCGH) is commonly used for CNV detection, but the microarray platform has a number of inherent limitations. Simulation of various sequencing methods with coverage ...

DNA copy number variation (CNV) has been recognized as an important source of genetic variation. Array comparative genomic hybridization (aCGH) is commonly used for CNV detection, but the microarray platform has a number of inherent limitations. Simulation of various sequencing methods with coverage ...
CNV-seq, a new method to detect copy number variat...

CNV-seq - National University of Singaporetiger.dbs.nus.edu.sg/cnv-seqBMC Bioinformatics 2009, 10:80 CNV-seq, a new method to detect copy number variation using high-throughput sequencing

BMC Bioinformatics 2009, 10:80 CNV-seq, a new method to detect copy number variation using high-throughput sequencing
tiger.dbs.nus.edu.sg/cnv-seq

CNV-seq, a new method to detect copy number variation ...https://bmcbioinformatics.biomedcentral.com/articles/10.1186/1471...Background. DNA copy number variation (CNV) has been recognized as an important source of genetic variation. Array comparative genomic hybridization (aCGH) is commonly used for CNV detection, but the microarray platform has a number of inherent limitations.

Background. DNA copy number variation (CNV) has been recognized as an important source of genetic variation. Array comparative genomic hybridization (aCGH) is commonly used for CNV detection, but the microarray platform has a number of inherent limitations.
bmcbioinformatics.biomedcentral.com/articles/10.11...

CNV-SEQ download | SourceForge.netsourceforge.net › … › Science & Engineering › Bio-InformaticsNov 25, 2016 · Download CNV-SEQ for free. CNV-SEQ is a software to estimate copy number variation using next-generation sequence data.

Nov 25, 2016 · Download CNV-SEQ for free. CNV-SEQ is a software to estimate copy number variation using next-generation sequence data.
CNV-SEQ download | SourceForge.netsourceforge.net

Cnv-seq - Research Computing Center Wikihttps://wiki.gacrc.uga.edu/wiki/Cnv-seqCategory. Bioinformatics Program On. zcluster Version. 0.2-7 Author / Distributor. Chao Xie and Martti T Tammi, please see http://tiger.dbs.nus.edu.sg/cnv-seq ...

Category. Bioinformatics Program On. zcluster Version. 0.2-7 Author / Distributor. Chao Xie and Martti T Tammi, please see http://tiger.dbs.nus.edu.sg/cnv-seq ...
wiki.gacrc.uga.edu/wiki/Cnv-seq

CNVSeq - UFRChttps://help.rc.ufl.edu/doc/CNVSeqCNVSeq website A new method to detect copy number variation using high-throughput sequencing. ...

CNVSeq website A new method to detect copy number variation using high-throughput sequencing. ...
help.rc.ufl.edu/doc/CNVSeq

CNV-seq - OMICtoolshttps://omictools.com/cnv-seq-toolCNV-seq provides a method based on a statistical model derived from aCGH that can be applied to low sequencing coverage. This application is combined to a model to compute the theoretical limit of resolution for given data at a desired confidence level. It was tested on …

CNV-seq provides a method based on a statistical model derived from aCGH that can be applied to low sequencing coverage. This application is combined to a model to compute the theoretical limit of resolution for given data at a desired confidence level. It was tested on …
omictools.com/cnv-seq-tool