Authors and Citation
Citation
Source: inst/CITATION
Laufer et al. Low-Pass Whole Genome Bisulfite Sequencing of Neonatal Dried Blood Spots Identifies a Role for RUNX1 in Down Syndrome DNA Methylation Profiles. Human Molecular Genetics (2020)
@Article{, author = {Benjamin I. Laufer and Hyeyon Hwang and Julia M. Jianu and Charles E. Mordaunt and Ian F. Korf and Irva Hertz-Picciotto and Janine M. LaSalle}, title = {Low-Pass Whole Genome Bisulfite Sequencing of Neonatal Dried Blood Spots Identifies a Role for RUNX1 in Down Syndrome DNA Methylation Profiles}, journal = {Human Molecular Genetics}, year = {2020}, doi = {10.1093/hmg/ddaa218}, url = {https://doi.org/10.1101/2020.10.12.335331}, }
Korthauer et al. Detection and accurate false discovery rate control of differentially methylated regions from whole genome bisulfite sequencing. Biostatistics (2018)
@Article{, author = {Keegan Korthauer and Sutirtha Chakraborty and Yuval Benjamini, and Rafael A Irizarry}, title = {Detection and accurate false discovery rate control of differentially methylated regions from whole genome bisulfite sequencing}, journal = {Biostatistics}, year = {2018}, doi = {10.1093/biostatistics/kxy007}, url = {https://doi.org/10.1093/biostatistics/kxy007}, }
Hansen et al. BSmooth: from whole genome bisulfite sequencing reads to differentially methylated regions. Genome Biology (2012)
@Article{, author = {Kasper D Hansen and Benjamin Langmead and Rafael A Irizarry}, title = {BSmooth: from whole genome bisulfite sequencing reads to differentially methylated regions}, journal = {Genome Biology}, year = {2012}, doi = {10.1186/gb-2012-13-10-r83}, url = {https://doi.org/10.1186/gb-2012-13-10-r83}, }