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User: Ming Tang

gravatar for Ming Tang
Ming Tang • 2.5k
Reputation:
2,520
Status:
Trusted
Location:
Houston/MD Anderson Cancer Center
Website:
http://crazyhottommy.b...
Twitter:
@tangming2005
Last seen:
4 days, 19 hours ago
Joined:
6 years, 3 months ago
Email:
t***********@gmail.com

I graduated from a "wet" lab in 2014. in 2012, I became interested in the bioinformatics field, especially the next generation sequencing field. I really love Unix command line, python and R programming languages. Now I am doing a computational biology postdoc at MD Anderson Cancer Center focusing on glioblastoma genomics.

Posts by Ming Tang

<prev • 300 results • page 1 of 30 • next >
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Comment: C: Interesting bioinformatics blogs (2017 edition)
... was googling something else and found this...thanks Vivek for promoting my blog. I now blog at https://divingintogeneticsandgenomics.rbind.io/ :) ...
written 11 weeks ago by Ming Tang • 2.5k
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Comment: C: No called peaks from macse 2 and the alignment rate 90%
... load the bam file or bigwig (make it from bam) to IGV, and visually check if there any enrichment in the genome or not. if not, the experiment failed most likely. ...
written 5 months ago by Ming Tang • 2.5k
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Comment: C: bedops -u does not work properly
... Thanks for the detailed answer. I used `<()` quite a bit as well :) learning to use more BEDOPS. ...
written 19 months ago by Ming Tang • 2.5k
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Comment: C: bedops -u does not work properly
... it is under-appreciated compared with bedtools, another good one :) ...
written 19 months ago by Ming Tang • 2.5k
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Comment: C: bedops -u does not work properly
... Now it makes sense. every input bed file should be sorted. with -u it does not give me errors, but just missing many overlapping entries. bedops is a very good tool BTW:) ...
written 19 months ago by Ming Tang • 2.5k
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Comment: C: bedops -u does not work properly
... yes, you are right. -ec is for checking error. but bedops -u should not expect sorted bed files, right? ...
written 19 months ago by Ming Tang • 2.5k
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Comment: C: bedops -u does not work properly
... even version: 2.4.30 (typical) is having the same issue. ...
written 19 months ago by Ming Tang • 2.5k
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bedops -u does not work properly
... bedops -u is not sorting the bed files bedops --version bedops citation: http://bioinformatics.oxfordjournals.org/content/28/14/1919.abstract version: 2.4.14 authors: Shane Neph & Scott Kuehn #dummy file: cat my.bed chr1 1 5 peak_1 chr1 2 6 pea ...
bed bedops intersect written 19 months ago by Ming Tang • 2.5k • updated 19 months ago by Alex Reynolds ♦ 28k
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Comment: C: Why do I get a weird copy number in the tumour?
... Hi Eric, may I ask how does the call command work? I have segment file output from sequenza. sequenza also gives a purity estimate. I want to scale the segment depth ratio by the tumor purity. The output of sequenaza segments is diff from cnvkit, so I am not sure how to use the call command. Thanks! ...
written 19 months ago by Ming Tang • 2.5k
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Answer: A: How to convert bam-readcount output to BED-VAF format
... Just for those who has the same problem, this may help https://github.com/sahilseth/bamreadcountr ...
written 22 months ago by Ming Tang • 2.5k

Latest awards to Ming Tang

Commentator 13 days ago, created a comment with at least 3 up-votes. For C: Depth of coverage
Epic Question 18 days ago, created a question with more than 10,000 views. For Extract Dendrogram Information From Heatmap Generated By Heatmap.2
Great Question 7 weeks ago, created a question with more than 5,000 views. For RNAseq heatmap.2 log2FC clustering
Teacher 5 months ago, created an answer with at least 3 up-votes. For A: Identification of functionally relevant regions from ChIP-seq experiments
Great Question 8 months ago, created a question with more than 5,000 views. For RNAseq heatmap.2 log2FC clustering
Popular Question 8 months ago, created a question with more than 1,000 views. For merge structural variant calls in bedpe format
Appreciated 8 months ago, created a post with more than 5 votes. For A: Peak callers for ChIP seq comparison
Great Question 9 months ago, created a question with more than 5,000 views. For RNAseq heatmap.2 log2FC clustering
Popular Question 13 months ago, created a question with more than 1,000 views. For merge structural variant calls in bedpe format
Popular Question 13 months ago, created a question with more than 1,000 views. For convert SNP calls to amino acid change
Good Answer 13 months ago, created an answer that was upvoted at least 5 times. For A: Peak callers for ChIP seq comparison
Good Answer 17 months ago, created an answer that was upvoted at least 5 times. For A: Peak callers for ChIP seq comparison
Popular Question 17 months ago, created a question with more than 1,000 views. For convert SNP calls to amino acid change
Great Question 17 months ago, created a question with more than 5,000 views. For RNAseq heatmap.2 log2FC clustering
Appreciated 19 months ago, created a post with more than 5 votes. For A: Peak callers for ChIP seq comparison
Popular Question 20 months ago, created a question with more than 1,000 views. For convert SNP calls to amino acid change
Student 22 months ago, asked a question with at least 3 up-votes. For what is the fastest way to sort big bam files? (300Gb)
Popular Question 22 months ago, created a question with more than 1,000 views. For convert SNP calls to amino acid change
Popular Question 23 months ago, created a question with more than 1,000 views. For Get all the translation start site for human genome
Popular Question 23 months ago, created a question with more than 1,000 views. For convert SNP calls to amino acid change
Appreciated 23 months ago, created a post with more than 5 votes. For A: Peak callers for ChIP seq comparison
Popular Question 23 months ago, created a question with more than 1,000 views. For any tutorials for structural variants filtering and prioritization
Popular Question 2.0 years ago, created a question with more than 1,000 views. For Get all the translation start site for human genome
Popular Question 2.1 years ago, created a question with more than 1,000 views. For Get all the translation start site for human genome
Good Question 2.1 years ago, asked a question that was upvoted at least 5 times. For what tools to visualize structural variants VCF files?
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