htslib | C library for high-throughput sequencing data formats | Genomics library
kandi X-RAY | htslib Summary
kandi X-RAY | htslib Summary
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Trending Discussions on htslib
QUESTION
I'm trying to choose unique regions for my Non-invasive Prenatal Testing (NIPT) project. I have done following steps:
- Create an artificial fasta file contains 50bp sequence. On each chromosome, the next sequence overlap 40bp from previous sequence
- Align and only chosen no mismatch sequence
I have a .sam file about 40gb, on the next step I try to merge all overlapping coordinates to one .bed file for using in samtools. This is my python script to do that:
...ANSWER
Answered 2022-Mar-14 at 04:13Hopefully this does the trick. Hard to know since I'm working without having the input file or knowing what the output should look like and can't really run the code to check for errors, but here's what I've tried to do:
- Eliminate
raw
and go straight to creatingtreat1
; and - Eliminate
treat2
and go straight to writing tobedfile
. I openedbedfile
right off the bat and everything in your program is done with that file open.
If this does what you need but still crashes, then perhaps you can read through each file twice to get last_coord
at the end of the treat1
and then read through it again to "recreate" each line of treat1
individually and apply it to defining what needs to be written into the file.
Without really knowing the details of what you're doing (I do not work anywhere close to a field that would apply samtools).
QUESTION
In bioinformatics we have the bgzip file, which is block-compressed, meaning that you can compress a file (let's say a CSV), and then if you want to access some data in the middle of that file, you can decompress only the middle chunk, rather than the entire file.
As is explained here, Arrow (and therefore Feather v2, the file format) seems to support chunked reads and writes, and also compression. However it isn't clear if the compression applies to the entire file, or if individual chunks can be decompressed. This is my questions: can we separately compress chunks of an Arrow/Feather v2 and then later decompress a single chunk without decompressing everything?
...ANSWER
Answered 2022-Feb-15 at 15:09QUESTION
I have the following .txt file:
...ANSWER
Answered 2021-Sep-29 at 13:30I would GNU AWK
following way, let file.txt
content be
QUESTION
Suppose I have a text file such as below. My question is how to read the lines starting with SN
in R. The whole file has over 10k rows but I just wanted the lines starting with SN
.
ANSWER
Answered 2021-Jun-30 at 15:38Using readLines()
and then grep
the SN's. Reads in the whole thing first, though.
QUESTION
// Compiled with GCC 7.3.0, x86-64 -g -O3 -std=gnu++11
// Tested on OS (1) Ubuntu 18.04 LTS, (2) Gentoo
int Listen(... socket)
{
char buffer[INT16_MAX];
. . .
. . . = recvfrom(socket, buffer, ....)
ParseMsg(buffer)
}
void ParseMsg(uint8_t *const msg)
{
. . .
uint16_t* word_arr = (uint16_t*)(msg+15); // if I changed 15 to 16 (aligned to uint16_t)
// the program doesn't crash
for(size_t i = 0 ; i < 30 ; ++i)
{
word_arr[i] = 1; // after some iterations (around 13) the program crashes with segmentation fault
// if i add a print statement inside the loop the program doesn't crash
}
// word_arr[20] = 1; // if I assign value not in loop the program doesn't crash
}
...ANSWER
Answered 2021-May-27 at 11:24The problem does underline in the alignment of the uint16_t
pointer (which should be 2), in combination with -O3
the compiler is trying to optimize your loop using vectorization (SIMD), hence trying to load unaligned argument to SSE registers.
This can explain why it works when:
- you change the offset from 15 to 16 - causes the
uint16_t
pointer to be aligned - with
-O2
- disable the vectorization - removing the loop / adding a print within the loop - also disable the vectorization
Please refer to the following link with a question similar to yours and some great elaborate answers:
c-undefined-behavior-strict-aliasing-rule-or-incorrect-alignment
QUESTION
I could not install htslib v1.12 with conda using either commands:
...ANSWER
Answered 2021-Apr-25 at 10:05The directives OP reference are from Anaconda Cloud, which are generic and miss the nuances that using specialized channels often entails. Specifically, Bioconda expects the following channel prioritization:
QUESTION
I am using htslib for extracting all the information contained in a VCF file in C++.
Currently, thanks to the VCF specification and the documentation in the file vcf.h, I have successfully extracted all the metadata information in the header (Meta-Information Lines), and most of the information contained in each row of the body of the file (Data Lines).
However, I don't know how to extract the genotype information (sample columns).
I am using example files from the 1000G project. This is an example of two rows of the file, it shows the Format field and two samples (The file has more than 1000 samples per each row, I would like to extract the data for all of them):
...ANSWER
Answered 2021-Feb-09 at 04:10I finally figured it out. There are some functions for doing this, depending on the type specified in the header for the format ID: the functions are inside of the vcf.h file in htslib:
QUESTION
I have a development laptop (Mint 19.3
), and a test server (Ubuntu 18.04.4 LTS
).
The laptop is Docker version 19.03.5, build 633a0ea838
, the server is Docker version 19.03.12, build 48a66213fe
I'm running Python 3.6 code inside the container, which uses subprocess
(code below) to create an sshfs mount to a third server, after which the python code walks through the mounted directory.
Everything works fine on my development laptop. But on the server, the directory mounts (and is seen with the mount
command) however cd'ing into the directory just hangs, and the Python code's subsequent walk
just hangs. (NOTE: The python code never crashes or errors out. It just hangs forever.)
HOWEVER, if I manually use the same sshfs command at the container's command line, the directory works fine.
I'm at a loss as to how to troubleshoot this.
===2020-09-25 UPDATE===
OK. Since the Python code uses subprocess, the sshfs mount is obviously available to any terminal windows that wants to use it.
I have tried accessing the mount from a new terminal window inside the container, but when I cd to the mount - the window just freezes.
Well, I left everything sitting overnight - and now when I try to cd into the mount ... it works. It's like the mount has to sit for hours before it will work.
Any ideas?
Python code
...ANSWER
Answered 2020-Dec-13 at 10:51I am assuming you want to mount some server's directory to container's filesystem using SSHFS. You could add that instruction to the Dockerfile:
QUESTION
I have a pipeline which uses a global singularity image and rule-based conda wrappers.
However, some of the tools don't have wrappers (i.e. htslib
's bgzip
and tabix
).
Now I need to learn how to run jobs in containers.
In the official documentation link it says:
"Allowed image urls entail everything supported by singularity (e.g.,
shub://
anddocker://
)."
Now I've tried the following image from singularity hub but I get an error:
minimal reproducible example:config.yaml
...ANSWER
Answered 2020-Sep-24 at 17:38Using another container solves the issue; however, the fact I'm getting errors from biocontainers
is troubling given that these are both very common and used as examples in the literature so I will award the top-answer to whomever can solve that specific issue.
As it were, the use of stackleader/bgzip-utility
solve the issue of actually running this rule in a container.
QUESTION
I want my Makefile to behave differently depending on whether I'm compiling on my own machine or inside a docker container. This is the Makefile:
...ANSWER
Answered 2020-Sep-15 at 02:18Make has two flavors of variable: simply expanded variables, and recursively expanded variables.
Here:
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