hisat | Fast spliced aligner with low memory requirements | Genomics library
kandi X-RAY | hisat Summary
kandi X-RAY | hisat Summary
HISAT is a fast and sensitive spliced alignment program for mapping RNA-seq reads. In addition to one global FM index that represents a whole genome, HISAT uses a large set of small FM indexes that collectively cover the whole genome (each index represents a genomic region of ~64,000 bp and ~48,000 indexes are needed to cover the human genome). These small indexes (called local indexes) combined with several alignment strategies enable effective alignment of RNA-seq reads, in particular, reads spanning multiple exons. The memory footprint of HISAT is relatively low (~4.3GB for the human genome). I have developed HISAT based on the Bowtie2 implementation to handle most of the operations on the FM index.
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QUESTION
I’am trying to classify bivariate point patterns into groups using spatstat. The patterns are derived from the whole slide images of lymph nodes with cancer. I’ve trained a neural network to recognize cells of three types (cancer “LP”, immune cells “bcell” and all other cells). I do not wish to analyse all other cells but use them to construct a polygonal window in the shape of the lymph node. Thus, the patterns to be analysed are immune cells and cancer cells in polygonal windows. Each pattern can have several 10k cancer cells and up to 2mio immune cells. The patterns are of the type “Small World Model” as there is no possibility of points laying outside the window.
My classification should be based on the position of the cancer cells in relation to the immune cells. E.g. most cancer cells are laying on the “islands” of immune cells but in some cases cancer cells are (seemingly) uniformly dispersed and there are only a few immune cells. In addition, the patterns are not always uniform across the node. As I’m rather new to spatial statistics I developed a simple and crude method to classify the patterns. Here in short:
- I calculated a kernel density of the immune cells with
sigma=80
because this looked “nice” for me.Den<-density(split(cells)$"bcell",sigma=80,window= cells$window)
(Should I have used e.g.sigma=bw.scott
instead?) - Then I created a tessellation image by dividing density range in 3 parts (here again, I experimented with the breaks to get some “good looking results”).
ANSWER
Answered 2021-Apr-29 at 09:21It seems you are trying to quantify the way in which the cancer cells are positioned relative to the immune cells. You could do this by something like
QUESTION
I have several non-tab separated files. I would like to merge them and create a single file with some information about all files.
I've tried this code but is not working when I use looping for
The original file is like
...ANSWER
Answered 2019-Jun-05 at 11:24Your example isn't 100% reproducible (what is samples
?), so I approximated.
QUESTION
I want to perform alignment using Hisat2 for single-ended thousands of samples and each sample distributed among different libraries.
I have modified this script (https://www.biostars.org/p/223404/#224169):
...ANSWER
Answered 2019-Apr-02 at 14:20Full path filenames shouldn't be dups, so I dropped the sort
.
I'm going to assume a reasonable number of files per sample.
For that -
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