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chaodengusc
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update the manual
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man/FisherButterfly.Rd

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data(FisherButterfly)
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}
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\keyword{ data }
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\keyword{ datasets }

man/SRR061157_k31.Rd

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\name{SRR061157_k31}
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\alias{SRR061157_k31}
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\docType{data}
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\title{k-mer counts of a metagenomic data}
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\description{The k-mer counts are based on a metagenome sequencing data from
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\title{\eqn{k}-mer counts of a metagenomic data}
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\description{The \eqn{k}-mer counts are based on a metagenome sequencing data from
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Human Microbiome Project with the accession number
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SRR061157. Only forward reads are used to generate the k-mer counts.}
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SRR061157. Only forward reads are used to generate the \eqn{k}-mer counts.}
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\references{
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Human Microbiome Project (\url{https://hmpdacc.org/}).
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}

man/SRR1301329_1M_base.Rd

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\name{SRR1301329_1M_base}
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\alias{SRR1301329_1M_base}
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\docType{data}
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\title{Coverage histogram of an exome sequencing data}
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\description{The coverage histogram is based on an exome sequencing data from
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Simons Foundation Autism Research Initiative with the accession number
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\title{Coverage histogram of a WES data}
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\description{The coverage histogram is based on an whole-exome sequencing (WES)
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data from Simons Foundation Autism Research Initiative with the accession number
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SRR1301329. One million reads are randomly sampled from the raw data to
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generate this coverage histogram.}
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\references{

man/SRR1301329_1M_read.Rd

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\name{SRR1301329_1M_read}
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\alias{SRR1301329_1M_read}
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\docType{data}
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\title{Read counts of an exome sequencing data}
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\description{The read counts are based on an exome sequencing data from
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Simons Foundation Autism Research Initiative with the accession number
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\title{Read counts of a WES data}
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\description{The read counts are based on an whole-exome sequencing (WES) data
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from Simons Foundation Autism Research Initiative with the accession number
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SRR1301329. One million reads are randomly sampled from the raw data to
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generate the read counts.}
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\references{

man/SRR1301329_base.Rd

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\name{SRR1301329_base}
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\alias{SRR1301329_base}
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\docType{data}
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\title{Coverage histogram of an exome sequencing data}
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\description{The coverage histogram is based on an exome sequencing data from
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Simons Foundation Autism Research Initiative with the accession number
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SRR1301329. Only forward reads are used to generate the coverage histogram.}
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\title{Coverage histogram of a WES data}
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\description{
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The coverage histogram is based on a whole-exome sequencing (WES)
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data from Simons Foundation Autism Research Initiative with the accession number
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SRR1301329. Only forward reads are used to generate the coverage histogram.
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}
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\references{
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Simons Foundation Autism Research Initiative (\url{https://www.sfari.org/}).
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}

man/SRR1301329_read.Rd

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\name{SRR1301329_read}
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\alias{SRR1301329_read}
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\docType{data}
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\title{Read counts of an exome sequencing data}
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\description{The read counts are based on an exome sequencing data from
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\title{Read counts of a WES data}
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\description{The read counts are based on a whole-exome sequencing data from
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Simons Foundation Autism Research Initiative with the accession number
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SRR1301329. Only forward reads are used to generate the read counts.}
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\references{

man/SRR611492.Rd

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\name{SRR611492}
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\alias{SRR611492}
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\docType{data}
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\title{Coverage histogram of a single-cell whole-genome sequencing data}
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\description{The coverage histogram is based on a single-cell whole-genome
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sequencing data through MALBAK protocol. The accession number of the raw data
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is SRR1301329. Only forward reads are used to generate the coverage histogram.}
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\title{Coverage histogram of a scWGS data}
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\description{
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The coverage histogram is based on a single-cell whole-genome
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sequencing data (scWGS) through MALBAK protocol. The accession number of the raw
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data is SRR1301329. Only forward reads are used to generate the coverage
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histogram.
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}
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\references{
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Zong, C., Lu, S., Chapman, A. R., & Xie, X. S. (2012). Genome-wide detection
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of single-nucleotide and copy-number variations of a single human cell.
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Science, 338(6114), 1622-1626.
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}
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\details{
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A two-column matrix.
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The first column is the frequency \eqn{j = 1,2,\dots}; and the second column

man/SRR611492_5M.Rd

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\name{SRR611492_5M}
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\alias{SRR611492_5M}
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\docType{data}
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\title{Coverage histogram of a single-cell whole-genome sequencing data}
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\description{The coverage histogram is based on a single-cell whole-genome
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sequencing data through MALBAK protocol. The accession number of the raw data
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is SRR1301329. Five million reads are randomly sampled from the raw data to
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generate this coverage histogram.}
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\title{Coverage histogram of a scWGS data}
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\description{
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The coverage histogram is based on a single-cell whole-genome
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sequencing (scWGS) data through MALBAK protocol. The accession number of the
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raw data is SRR1301329. Five million reads are randomly sampled from the raw
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data to generate this coverage histogram.
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}
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\references{
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Zong, C., Lu, S., Chapman, A. R., & Xie, X. S. (2012). Genome-wide detection
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of single-nucleotide and copy-number variations of a single human cell.

man/ShakespeareWordHist.Rd

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\name{ShakespeareWordHist}
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\alias{ShakespeareWordHist}
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\name{Shakespeare}
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\alias{Shakespeare}
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\docType{data}
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\title{Shakespeare's word type frequencies}
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\description{The Shakespeare's word type frequencies data was from
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library(preseqR)
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##load data
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data(ShakespeareWordHist)
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data(Shakespeare)
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}
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\keyword{ data }
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\keyword{ datasets }

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