* see Methods section for how the bisulfite conversion rate is calculated Sample flag: LowBS: sample has low bisulfite conversion rate (<0.95); LowCov: sample has low mean coverage (<6.0)
Terms of use: If you use this resource, please cite us!
The Smith Lab at USC has developed and is owner of all analyses and associated browser tracks from
the MethBase database (e.g. tracks displayed in the "DNA Methylation" trackhub on the UCSC Genome Browser).
Any derivative work or use of the MethBase resource that appears in published literature must cite
the most recent publication associated with Methbase (see "References" below).
Users who wish to copy the contents of MethBase in bulk into a publicly available resource
must additionally have explicit permission from the Smith Lab to do so.
We hope the MethBase resource can help you!
Display Conventions and Configuration
The various types of tracks associated with a methylome follow the
display conventions below.
Green intervals represent partially methylated region; Blue intervals
represent hypo-methylated regions; Yellow bars represent methylation
levels; Black bars represent depth of coverage; Purple intervals
represent allele-specific methylated regions; Purple bars represent
allele-specific methylation score; and red intervals represent
hyper-methylated regions.
Methods
All analysis was done using a bisulfite sequnecing data analysis
pipeline MethPipe developed in the Smith lab at USC.
Mapping bisulfite treated reads: Bisulfite treated reads are mapped
to the genomes with the rmapbs program (rmapbs-pe for pair-end
reads), one of the wildcard based mappers. Input reads are filtered by
their quality, and adapter sequences in the 3' end of reads are
trimmed. Uniquely mapped reads with mismatches below given threshold
are kept. For pair-end reads, if the two mates overlap, the
overlapping part of the mate with lower quality is clipped. After
mapping, we use the program duplicate-remover to randomly select one
from multiple reads mapped exactly to the same location.
Estimating methylation levels: After reads are mapped and filtered,
the methcounts program is used to obtain read coverage and estimate
methylation levels at individual cytosine sites. We count the number
of methylated reads (containing C's) and the number of unmethylated
reads (containing T's) at each cytosine site. The methylation level
of that cytosine is estimated with the ratio of methylated to total
reads covering that cytosine. For cytosines within the symmetric CpG
sequence context, reads from the both strands are used to give a
single estimate.
Estimating bisulfite conversion rate: Bisulfite conversion rate is
estimated with the bsrate program by computing the fraction of
successfully converted reads (read out as Ts) among all reads mapped
to presumably unmethylated cytosine sites, for example, spike-in
lambda DNA, chroloplast DNA or non-CpG cytosines in mammalian
genomes.
Identifying hypo-methylated regions: In most mammalian cells, the
majority of the genome has high methylation, and regions of low
methylation are typically more interesting. These are called
hypo-methylated regions (HMR). To identify the HMRs, we use the hmr
which implements a hidden Markov model (HMM) approach taking into
account both coverage and methylation level information.
Identifying hyper-methylated regions: Hyper-methylated regions
(HyperMR) are of interest in plant methylomes, invertebrate
methylomes and other methylomes showing "mosaic methylation"
pattern. We identify HyperMRs with the hmr_plant program for those
samples showing "mosaic methylation" pattern.
Identifying partially methylated domains: Partially methylated
domains are large genomic regions showing partial methylation
observed in immortalized cell lines and cancerous cells. The pmd
program is used to identify PMDs.
Identifying allele-specific methylated regions: Allele-Specific
methylated regions refers to regions where the parental allele is
differentially methylated compared to the maternal allele. The
program allelicmeth is used to allele-specific methylation score
can be computed for each CpG site by testing the linkage between
methylation status of adjacent reads, and the program amrfinder is
used to identify regions with allele-specific methylation.
For more detailed description of the methods of each step, please
refer to the reference by Song et al. For instructions on how to use
MethPipe, you may obtain the MethPipe Manual.
Credits
The raw data were produced by Lister R et al, Zeng J et al, Schroeder DI et al. The data analysis were
performed by members of the Smith lab.
If you use this resource, please cite us! The Smith Lab at USC has developed and is owner of all analyses and associated browser tracks from the MethBase database (e.g. tracks displayed in the "DNA Methylation" trackhub on the UCSC Genome Browser). Any derivative work or use of the MethBase resource that appears in published literature must cite the most recent publication associated with Methbase (see "References" below). Users who wish to copy the contents of MethBase in bulk into a publicly available resource must additionally have explicit permission from the Smith Lab to do so. We hope the MethBase resource can help you!
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