Download Supplementary Figure S3 (ppt 134K)

Survey
yes no Was this document useful for you?
   Thank you for your participation!

* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project

Document related concepts

X-inactivation wikipedia , lookup

Cell-free fetal DNA wikipedia , lookup

Vectors in gene therapy wikipedia , lookup

Cancer epigenetics wikipedia , lookup

Pathogenomics wikipedia , lookup

Extrachromosomal DNA wikipedia , lookup

Non-coding DNA wikipedia , lookup

Oncogenomics wikipedia , lookup

Essential gene wikipedia , lookup

Polycomb Group Proteins and Cancer wikipedia , lookup

Site-specific recombinase technology wikipedia , lookup

Therapeutic gene modulation wikipedia , lookup

Quantitative trait locus wikipedia , lookup

Nutriepigenomics wikipedia , lookup

Genome evolution wikipedia , lookup

Metagenomics wikipedia , lookup

Genome (book) wikipedia , lookup

Genomic imprinting wikipedia , lookup

Ridge (biology) wikipedia , lookup

Designer baby wikipedia , lookup

Gene wikipedia , lookup

History of genetic engineering wikipedia , lookup

Epigenetics of human development wikipedia , lookup

Microevolution wikipedia , lookup

Artificial gene synthesis wikipedia , lookup

Biology and consumer behaviour wikipedia , lookup

Minimal genome wikipedia , lookup

Gene expression profiling wikipedia , lookup

RNA-Seq wikipedia , lookup

Transcript
2.1
2.0
1.9
Female:male
read ratio
1.5
1.1
1.0
0.9
0.5
Gene name
Supplementary Figure S3. Male to female read depth ratios reflects relative DNA copy number for both X-linked and autosomal genes
The X-linked genes HPRT1 and KDM6A gave twice (read ratio close to 2) the number of standardised reads in female vs male DNA samples. By contrast, the
remaining 32 autosomal genes gave similar read numbers from male and female samples. It is noteworthy that the outlying genes CYP2D6 and PTEN (F:M
read ratios >1.1) were found to exhibit sample-specific read number variation on further analysis (see Supplementary figure S4).
Box plots show the median (central dark line), upper and lower quartiles (box). Whiskers mark the lowest & highest data points still within 1.5 IQR of the
lower and upper quartiles respectively . Any data not included between the whiskers is plotted as an outlier with a dot or star.