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SRX6422865: GSM3935004: disease rep2 [W_006]; Homo sapiens; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 55.5M spots, 4.2G bases, 1.4Gb downloads

Submitted by: NCBI (GEO)
Study: Machine Learning Classifiers for Endometriosis Using Transcriptomics and Methylomics Data [Transcriptomics]
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We experimented how well various supervised machine learning methods such as decision tree, partial least squares discriminant analysis (PLSDA), support vector machine and random forest perform in classifying endometriosis from the control samples trained on both transcriptomics and methylomics data. The assessment was done from two different perspectives for improving classification performances: (a) implication of three different normalization techniques, and (b) implication of differential analysis using the generalized linear model (GLM). We concluded that an appropriate machine learning diagnostic pipeline for endometriosis should use TMM normalization for transcriptomics data, and quantile or voom normalization for methylomics data, GLM for feature space reduction and classification performance maximization. Overall design: Total 38 RNA-seq samples were analyzed where 22 were control and 16 were disease samples Please note that the GSE134052 records represent the methylomics data.
Sample: disease rep2 [W_006]
SAMN12239239 • SRS5079654 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Total RNA was extracted with the Qiagen RNeasy kit following storage in RNAlater Libraries were constructed following the manufacturer's protocol with reagents supplied in Illumina's TruSeq mRNA stranded library preparation kit.  The method involves mRNA enrichment from total RNA followed by RNA fragmentation and conversion to double-stranded cDNA using random hexamers.
Links:
Runs: 1 run, 55.5M spots, 4.2G bases, 1.4Gb
Run# of Spots# of BasesSizePublished
SRR966199055,534,6784.2G1.4Gb2019-07-18

ID:
8507430

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