alisman
alisman
It would be nice if the run method accepted a callback or returned a promise so that associating calls and emitted events could be abstracted away. This was easy enough...
We very often want to use libraries like lodash in compute intensive routines that would be good to run in workers. Have you thought about how to solve this problem?
I am using a file called Summary.MD to configure navigation. I think this might be leftover from gitbook. But it actually works with retype although it isn't documented anywhere. What's...
Retries are an essential part of e2e in order to deal with flakey tests. When a screenshot is missing, the framework creates a new one and saves it. This causes...
**Let start by saying thank you. This library looks amazing, well documented, and I really want to use it. But I don't get this one bit. Suppose I have a...
There were a number of localdb e2e failures in 5.0 related to annotation filter. Best I could tell, this has to do with the filtering endpoint handling of structural variants....
https://www.cbioportal.org/patient?sampleId=TCGA-04-1357-01&studyId=ov_tcga_pub When we click on a row in an alteration table, the IGV focuses to that alterations location, but we don't mark the row as selected. It's quite difficult to...
[Example query](https://www.cbioportal.org/results/comparison?cancer_study_list=coadread_tcga_pub&cancer_study_id=coadread_tcga_pub&genetic_profile_ids_PROFILE_MUTATION_EXTENDED=coadread_tcga_pub_mutations&genetic_profile_ids_PROFILE_COPY_NUMBER_ALTERATION=coadread_tcga_pub_gistic&Z_SCORE_THRESHOLD=2.0&case_set_id=coadread_tcga_pub_nonhypermut&gene_list=KRAS%20NRAS%20BRAF&gene_set_choice=user-defined-list&comparison_subtab=alterations) The frequencies listed in the Altered group and Unaltere group columns are percentage would appear to be a percentage of the overall number of samples in these respective...
For example gene ABLIM1 which returns profiled count of 23 when only 12 unique samples have been submitted as part of altered group. The calulation of profiled samples is off....
Oncprint mysteriously shows genes "detected as fusion partners" in oncoprint tooltip despite the absence of structural variant data. 