Mapping was performed on the state level using ESRI's ArcMap GIS software (ESRI, Redlands, WA).
Mapping was performed using Bowtie270 tool with default parameters.
Similar sequential mapping was performed for snRNA, scRNA, tRNA, rRNA, and piRNAs.
sQTL mapping was performed separately for each condition and merging both populations.
Mapping was performed using Bismark to GRCm38 builds for the mouse genome25.
Linkage mapping was performed on two mapping populations: Salinas 88 × La Brillante (S88 × LB) and Pavane × Parade (Pav × Par).
Mapping was performed by stimulating adjacent electrode pairs and recording CCEPs from the remainder of the electrode array.
Human T cell epitope mapping was performed by applying the computational EpiMatrix™ algorithm (EpiVax, Inc).
As shown in Figure 3a, SiO2 NTs are randomly oriented, and a selected area EDS mapping was performed on the region within the yellow box.
At the time the mapping was performed, BWA 0.5 was the latest stable version of BWA, as 0.6 and 0.7 were being released with frequent bug fixes.
In this oblique position, color Doppler mapping was performed to detect blood flow within the consolidation.
