When considering each combination of read layout, length and fusion finding algorithm, we found that JAFFA with 100 bp paired-end reads produced the highest number of true positives, with a total of 27.
Face validity for our measure was evaluated during the pilot testing of the questionnaire when fifteen health professionals were invited to provide feedback on the content of the instrument including: wording, layout, length, questions asked and also if there were any important questions missing.
The typical number of WAPs per carriage is two but this can vary depending on the layout and length of the carriage.
The thickness effects of high-tensile-stress contact etch stop layer (HS CESL) and impact of layout geometry (length of diffusion and gate width) on mobility enhancement of 〈100〉/(1009090 nm SOI nMOSFETs were studied in detail.
Here, we present a multi-electrode system made from biocompatible material that is electrically and mechanically stable, and employs design features allowing flexibility in the geometric layout and length of the individual electrodes within the array.
Furthermore, participants commented on the format of the questionnaire including response categories, layout, and length of the survey.
The discussion guide was structured to concentrate on the following key areas to determine face and content validity: 1) design of survey (layout, order, length); 2) language (translation, clarity, vocabulary, brevity and focus); 3) applicability and specificity of the items.
When we examined the optimal sequencing read layout and length for fusion detection, we found that JAFFA was the most sensitive on 100 bp pair-end reads compared with any other scenario or tool.
Other components permit accurate identification of many tissue types such as brain, liver and bladder, even though the RNA-seq data for these tissues had been generated in at least six different laboratories, with often quite pronounced technical differences (for example, in sequencer model, read layout, read length, and total number of reads, Figure 1c).
Because we know that the order matters, we set an order that first includes the preparation variability we can account for (layout, read length, RNA extraction method and number of raw reads) and then includes the part of the variability we cannot account for (the study and tissue types).
Cut the louver vane frame, again, using the layout for lengths and angles.
