gtf | gtf - a useful set of Golang Template Functions | Widget library
kandi X-RAY | gtf Summary
kandi X-RAY | gtf Summary
gtf is a useful set of Golang Template Functions. The goal of this project is implementing all built-in template filters of Django & Jinja2.
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gtf Key Features
gtf Examples and Code Snippets
def load_annotations(self):
assert self.data_type == 'mot'
gt_filename = os.path.join(self.data_root, self.seq_name, 'gt', 'gt.txt')
self.gt_frame_dict = read_results(gt_filename, self.data_type, is_gt=True)
self.gt_i
Community Discussions
Trending Discussions on gtf
QUESTION
I am mapping and counting sequences that are mixed from two species. I have two rules in my pipeline because each specie has it's own GTF file. I would like to be able to merge this into one rule, and then have the specie wildcard dictate which GTF file to use (using a dictionary for example). These are the rules:
...ANSWER
Answered 2021-Dec-27 at 14:23Figured it out. Need to use lambda:
QUESTION
I am trying to resume training monkAI pytorch retinanet. I have loaded with .pt file instead of actual model. The changes are made in Monk_Object_Detection/5_pytorch_retinanet/lib/train_detector.py, check for '# change' in the places where its modified.
...ANSWER
Answered 2021-Dec-22 at 22:43I found this by simply googling your problem:
retinanet.load_state_dict(torch.load('filename').module.state_dict())
The link to the discussion is here.
QUESTION
I have a dataset that looks something like this:
...ANSWER
Answered 2021-Dec-19 at 09:00Use:
QUESTION
Complete rust beginner here coming from python. I would like to use rust-polars to read a compressed GTF (*.gtf.gz) file:
...ANSWER
Answered 2021-Oct-19 at 14:21Hi there are a few questions here at once. I will try to answer the ones I can.
How to tell Polars that the file is compressed?
You don't have to. You only have to compile polars with the decompress
or decompress-fast
feature flag. (The firs one is rust native, the latter needs a c-compiler).
How to parse Categorical columns
You set the schema to DataType::Categorical
, or you first parse as Utf8
and then cast later.
QUESTION
I have a very simple one liner that works almost perfectly. I want to add a new column to a file that says "non coding or coding" depending on conditions on columns 12 and 3 (if column 12 has substring RNA or mir- and/or column 3 == "pseudogene then column 1 should read non-coding else coding).
...ANSWER
Answered 2021-Sep-02 at 03:57You can (effectively) prepend a new column by converting $1
into something OFS $1
. You aren't really creating a new column ($2
still refers to the original second column and $1
refers to "both" new columns) but that is not important in this case:
QUESTION
I'm beginner in Bash Scripting and I need to assign to a variable a custom command output,not the entire command just a part of it.Is there a way I can do that?
The command:
ANSWER
Answered 2021-Aug-11 at 11:53You can enclose your command in backticks to store its output:
QUESTION
I have a data set where I have a few thousand records. The columns are acct number, code, data.
I need to sort the entire rows based on the code(column 2) if they have the same acct number(column1). so something like this.
...ANSWER
Answered 2021-Jul-02 at 22:35The last question you linked made your question clearer. Create an Order
column, sort by it, and drop it. You can determine the order in the dictionary.
QUESTION
I am using a cellranger mkref and faced with a strange python problem with GTF (custom gtf file):
...ANSWER
Answered 2021-May-26 at 21:50Python 3 treats strings of bytes as a different object from strings of characters. The distinction matters, since a given string of characters can be encoded to bytes in different ways. E.g. in UTF-8, ä
is the two bytes c3 a4
(in hex), while in ISO-8859-1 (Latin 1), it's just the single byte e4
.
Like the comment from @Theophrastus says, subprocess.check_output()
returns bytes, matching the low-level API. You need to decode it to characters based on what the expected encoding is. E.g.
QUESTION
I am using a cellranger mkref and faced with a strange python problem with GTF (custome gtf):
...ANSWER
Answered 2021-Jun-01 at 20:27I encountered the same issue. The problem was in duplicated IDs in my GTF file. Removing those duplicates solved the issue. See the discussion on Cellranger GitHub: https://github.com/10XGenomics/cellranger/issues/125
QUESTION
I have a snakemake pipeline that looks like this:
...ANSWER
Answered 2021-Apr-29 at 23:51The expand
function returns a list. By setting the input files to a list instead of a string, you are confusing the script. For defining r1 and r2, you should use something that returns a string instead. I would suggest the string's format()
function or an f-string.
Change:
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