- You are assisting Tu.
- Tu is an senior bioinformatics engineer, proficient in Python and R and their ecosystems.
- Tu values "Slow is Fast," focusing on: reasoning quality, scientific rigour, and long-term maintainability—not short-term speed.
- Your core objectives:
- Act as a strong reasoning, strong planning coding assistant, delivering high-quality solutions and implementations with minimal back-and-forth;
- Prioritize getting it right the first time; avoid superficial answers and unnecessary clarifications.
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| #!/bin/bash | |
| # ucloud-connect: Update the "ucloud" block in ~/.ssh/config with a new port | |
| # number (prompted, or passed as an argument), ensure the remaining settings | |
| # are correct (incl. LocalForward), and connect to ucloud via VSCode | |
| # Remote-SSH. | |
| # | |
| # Network constraint: ssh.cloud.sdu.dk is reached through a ProxyJump, and | |
| # local port 8888 is forwarded to localhost:8888 on the ucloud VM. Services | |
| # listening on the VM (e.g. Jupyter) are therefore available locally at |
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| Baby Sleep Assistant Skill | |
| Role | |
| You are the dedicated sleep assistant for my 10-month-old baby. | |
| Your role is not to enforce generic sleep training rules, but to continuously learn my baby’s unique sleep patterns through longitudinal observation. | |
| Treat this as an ongoing research project rather than a one-time consultation. |
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| {"name":"coder_python","settings":"{\"settings\":\"{\\n \\\"workbench.colorTheme\\\": \\\"Visual Studio Dark\\\",\\n \\\"extensions.autoUpdate\\\": false,\\n \\\"workbench.startupEditor\\\": \\\"none\\\",\\n \\\"tabnine.experimentalAutoImports\\\": true\\n}\\n\"}","extensions":"[{\"identifier\":{\"id\":\"eamodio.gitlens\",\"uuid\":\"4de763bd-505d-4978-9575-2b7696ecf94e\"},\"displayName\":\"GitLens — Git supercharged\"},{\"identifier\":{\"id\":\"ms-python.debugpy\",\"uuid\":\"4bd5d2c9-9d65-401a-b0b2-7498d9f17615\"},\"displayName\":\"Python Debugger\"},{\"identifier\":{\"id\":\"ms-python.python\",\"uuid\":\"f1f59ae4-9318-4f3c-a9b5-81b2eaa5f8a5\"},\"displayName\":\"Python\"},{\"identifier\":{\"id\":\"ms-toolsai.jupyter\",\"uuid\":\"6c2f1801-1e7f-45b2-9b5c-7782f1e076e8\"},\"displayName\":\"Jupyter\"},{\"identifier\":{\"id\":\"ms-toolsai.jupyter-keymap\",\"uuid\":\"9f6dc8db-620c-4844-b8c5-e74914f1be27\"},\"displayName\":\"Jupyter Keymap\"},{\"identifier\":{\"id\":\"ms-toolsai.jupyter-renderers\",\"uuid\":\"b15 |
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| library(ComplexHeatmap) | |
| count_matrix # if your data is called count_matrix | |
| # Read data | |
| se <- readRDS("data/se.rds") | |
| count_matrix <- assay(se) | |
| # Data transformation | |
| count_matrix_log2 <- log2(count_matrix + 1) |
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| counttable_merge_library_fun <- function(counttable_data = ..., | |
| lib_to_merge_vector = ...){ | |
| lib_id <- counttable_data %>% colnames() %>% str_extract("lib\\d{1,}") | |
| merged_counttable <- sapply(lib_to_merge_vector, function(one_lib_id_to_merge){ | |
| merged_counts <- counttable_data %>% select((lib_id == one_lib_id_to_merge) %>% which()) %>% rowSums() | |
| merged_counts_df <- tibble(one_lib_id_to_merge = merged_counts) | |
| return(merged_counts_df) | |
| }) # The function to merge libs for counttable ----------------- | |
| # list tidy | |
| MergedLib <- do.call(rbind.data.frame, merged_counttable) %>% t() %>% as.data.frame() %>% tibble() |
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| library(dplyr) | |
| a_vector_of_genes <- c("AP005212.4", "Z98257.1", "U62317.4", "CLIC4P3", "PGLYRP2", "NEK4P1") | |
| a_vector_of_cleaned_genes <- data.frame(a_vector_of_genes) %>% filter(!a_vector_of_genes %>% stringr::str_detect("\\d{1,}P$|\\d{1,}P\\d{1,}$|\\.|-AS\\d{1}|-DT")) %>% pull(a_vector_of_genes) |
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| # Cluster analysis in R | |
| # inspired by Dima Gorenshteyn, DataCamp | |
| ## standardize data | |
| df_st <- scale(df) | |
| ## Hierachical clustering | |
| d <- dist(df) | |
| hc <- hclust(d, "method") # method %in% c("complete", "average", "single") | |
| c <- cutree(hc, h = the_height) # h: the height to cut the tree # assign cluster |
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| pos_n_max <- pos_data %>% pull(feature) %>% stringr::str_match("\\d{1,}") %>% max() | |
| neg_feature_n <- neg_data %>% pull(feature) %>% stringr::str_match("\\d{1,}") | |
| neg_data %>% mutate(feature = paste0("F", neg_feature_n + pos_n_max)) |
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| # First install R (https://www.r-project.org/) and RStudio(https://rstudio.com/) | |
| # Install enrichR | |
| install.packages("enrichR") | |
| # Load enrichR | |
| library(enrichR) | |
| # Get your gene list, e.g. type by hand | |
| Inflammatory_markers <- c("IL13","MMP12","IL22","NTRK1", "CCL17", "IL36A", "ICOS", "CCL18", "ALOX15", "CCL1", "CCR5", "IL13RA2", "IL19", "CCR7","CCL20", "CCR4","CCR2","CCL11","CCL22","CCR8","CCL19","CCL26","CCL3") |