Bioinformatics analysis of single cell sequencing data once scrna seq data is generated several options are available for downstream bioinformatics analysis.
Single cell methylation sequencing.
Single cell dna methylome sequencing quantifies dna methylation there are several known types of methylation that occur in nature including 5 methylcytosine 5mc 5 hydroymethylcytosine 5hmc 6 methyladenine 6ma and 4mc 4 methylcytosine 4mc.
It is essential for maintenance of cellular identity and is associated with a number of key processes including genomic imprinting x chromosome inactivation repression.
The key advantage of targeted single cell bisulfite based analyses is that this approach focuses on regions of interest thus greatly reducing the costs.
12 534 2017.
Single cell splicing variation during endoderm differentiation.
Genome wide base resolution mapping of dna methylation in single cells using single cell bisulfite sequencing scbs seq.
Dna methylation is a crucial layer of epigenetic regulation during mammalian embryonic development 1 3 although the dna methylome of early human embryos has been analyzed 4 6 some of the key features have not been addressed thus far here we performed single cell dna methylome sequencing for human preimplantation embryos and found that tens of thousands of genomic loci exhibited de novo dna.
Here we present a procedure for single cell locus specific bisulfite sequencing slbs allowing to directly measuring dna methylation patterns in single cells and estimate epimutation rates.
We applied parallel single cell methylation and transcriptome sequencing scm t seq to differentiating induced pluripotent stem ips cells from one cell line joxm 1 of the human induced pluripotent stem cell initiative hipsci 15 16 we profiled 93 cells from 2 different cell types namely cells in the ips state ips and.
Furthermore they present a bioinformatic method for analyzing low coverage methylome data and apply this technique to inferring epigenomic cell state dynamics in pluripotent and differentiating cells.
It explores roles of target gene methylations in the pathogenesis of diseases as well.
Describe a method for dna methylation sequencing in very small cell populations μwgbs and single cells scwgbs.
Importantly this book aims to apply the measurement of single cell sequencing and methylation for clinical diagnosis and treatment and to understand clinical values of those parameters and to headline and foresee the potential values of the application of single cell sequencing in non cancer diseases.
First the raw sequencing reads need to be aligned to the reference genome cell barcodes need to be detected and reads or umis originating from the rna of the same cell need to be assigned to genes and quantified.