Data preparation: Bulk RNA-seq data

MY Matthew D. Young
TM Thomas J. Mitchell
LC Lars Custers
TM Thanasis Margaritis
FM Francisco Morales-Rodriguez
KK Kwasi Kwakwa
EK Eleonora Khabirova
GK Gerda Kildisiute
TO Thomas R. W. Oliver
RK Ronald R. de Krijger
MH Marry M. van den Heuvel-Eibrink
FC Federico Comitani
AP Alice Piapi
EB Eva Bugallo-Blanco
CT Christine Thevanesan
CB Christina Burke
EP Elena Prigmore
KA Kirsty Ambridge
KR Kenny Roberts
FB Felipe A. Vieira Braga
TC Tim H. H. Coorens
IV Ignacio Del Valle
AW Anna Wilbrey-Clark
LM Lira Mamanova
GS Grant D. Stewart
VG Vincent J. Gnanapragasam
DR Dyanne Rampling
NS Neil Sebire
NC Nicholas Coleman
LH Liz Hook
AW Anne Warren
MH Muzlifah Haniffa
MK Marcel Kool
SP Stefan M. Pfister
JA John C. Achermann
XH Xiaoling He
RB Roger A. Barker
AS Adam Shlien
OB Omer A. Bayraktar
ST Sarah A. Teichmann
FH Frank C. Holstege
KM Kerstin B. Meyer
JD Jarno Drost
KS Karin Straathof
SB Sam Behjati
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Each bulk RNA-seq sample required two pieces of information: fragment counts per gene and the effective length of each gene. As described above, gene counts for this paper were mostly generated using the Rail-RNA pipeline39 and effective gene lengths as the sum of unique exonic bases per gene. However, fragment counts and effective gene lengths can be calculated in any way.

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