Hayley
Hayley
Dear RoseTTAFold Team, Hi, I'm a user! I tried to predict a large protein (>2500 amino acids) using RoseTTAFold in Linux server. But, I got this message. [log/make_msa.stderr] ``` ...skipping......
Dear MAVIS team. Hi I'm Oh. I have two questions. Q1. If I change reference or annotated files, can I visualize viral integrations? Q2. I found the following fusion. (the...
Dear @tobiasrausch, Hi. I'm Oh. I executed the delly for Germline CNV calling. I want to ask about the genotype of my called CNVs (c1.cnv.bcf), or merge the calls (merged.bcf)....
Dear SpaceXR team. Hi, I really appreciate this wonderful tool. Then, I have a question. If I get the devoluted results using RCTD, can I use it to cluster spots...
Dear velocyto team I’m a user of velocyto. I have a question. I have a visium sequenced data and I attached the detailed information.  https://www.10xgenomics.com/support/spatial-gene-expression-ffpe/documentation/workflows/cytassist-ffpe/steps/experimental-design-and-planning In this setting, can...
Dear BayesSpace Team, Thank you this beautiful tool. I'm going to use the results of spatial enhance data. Then, each spot will be divided into 6 subspots. In this case,...
Dear STUtility team. When I plot the feature plots using Seurat, and STUtility package. I got two following images that is flipped. can I flip my STUtility derived feature plot...
Dear @sqjin Hi, I'm a big fan of your program. However, I have just two questions. # Q1. Spot diameter The spot diameter of 10X visium is 55um. This is...
Dear @sqjin Thank you for providing this valuable resource. I have two questions, Q1. I want to understand the impact of stroma spots on neighboring cells. In such cases, is...