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Comment: C: How to tell bloodtype from SNPs data?
3.7 years ago by eric.kern13 ▴ 240
0
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1
reply
13k
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Comment: A: Unable to install XLconnect package in R studio version 3.2.1
updated 5.0 years ago by 44k • written 9.3 years ago by ▴ 240
4
votes
1
reply
12k
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Answer: A: Downloading a Small VCF File
updated 5.0 years ago by 44k • written 9.3 years ago by ▴ 240
0
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1
reply
22k
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Comment: C: Using Seurat 3 Data for Pseudotime Analysis in Monocle 3
5.1 years ago by eric.kern13 ▴ 240
0
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0
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1.5k
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Comment: C: Help setting up lncRNA-screen from github
5.9 years ago by eric.kern13 ▴ 240
8
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0
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58k
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Comment: C: How To Write Data In A Granges Object To A Bed File.
6.1 years ago by eric.kern13 ▴ 240
0
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0
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8.8k
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Answer: A: Adapter/Linker/Primer Sequence Database?
6.3 years ago by eric.kern13 ▴ 240
2
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2
replies
2.8k
views
Mappability Scores from bigWigAverageOverBed all zero
sequencing
updated 2.2 years ago by 44k • written 9.2 years ago by ▴ 240
1
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0
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2.2k
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Answer: A: Overdispersion for single cell RNA seq experiments
6.8 years ago by eric.kern13 ▴ 240
0
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0
replies
3.3k
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Comment: C: Question about dbSNP rs #s
7.1 years ago by eric.kern13 ▴ 240
0
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1
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27k
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Comment: C: Duplicated Reads In Rna-Seq Experiment
7.3 years ago by eric.kern13 ▴ 240
0
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0
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57k
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Comment: C: Should We Remove Duplicated Reads In Rna-Seq ?
7.3 years ago by eric.kern13 ▴ 240
0
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1
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2.2k
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What happens during seed stitching when STAR initially gets the wrong MMP?
rna-seq STAR
updated 7.5 years ago by 5.8k • written 7.5 years ago by ▴ 240
0
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0
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2.1k
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Comment: C: Retrieve all genes under a mammalian phenotype ontology term
7.6 years ago by eric.kern13 ▴ 240
2
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4
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2.1k
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Retrieve all genes under a mammalian phenotype ontology term
R GO Mammalian Phenotype Ontology Biomart
updated 7.6 years ago by ★ 2.1k • written 7.6 years ago by ▴ 240
0
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0
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2.1k
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Comment: C: Retrieve all genes under a mammalian phenotype ontology term
7.6 years ago by eric.kern13 ▴ 240
0
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0
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4.1k
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Comment: C: cell surface receptor genes
8.1 years ago by eric.kern13 ▴ 240
1
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1
reply
3.9k
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Interpreting ANNOVAR allele frequency output
sequencing genome
8.1 years ago by eric.kern13 ▴ 240
1
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0
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3.9k
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Answer: A: Interpreting ANNOVAR allele frequency output
8.1 years ago by eric.kern13 ▴ 240
0
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0
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2.4k
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Comment: C: EdgeR or Ttest/ANOVA for non normal RNAseq data?
8.6 years ago by eric.kern13 ▴ 240
0
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0
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5.6k
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Comment: C: Can someone help me with imputation of missing SNPs using beagle 4?
8.6 years ago by eric.kern13 ▴ 240
0
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0
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2.1k
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Answer: Answer: Comparing results from ADMIXTURE and EIGENSTRAT
updated 2.2 years ago by 44k • written 9.1 years ago by ▴ 240
1
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0
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13k
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Comment: C: Should I use the p-value or q-value for pathway analysis in DAVID?
9.2 years ago by eric.kern13 ▴ 240
1
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0
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2.8k
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Comment: C: Mappability Scores from bigWigAverageOverBed all zero
9.2 years ago by eric.kern13 ▴ 240
1
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1
reply
2.8k
views
Answer: Answer: Mappability Scores from bigWigAverageOverBed all zero
updated 2.2 years ago by 44k • written 9.2 years ago by ▴ 240
2
votes
0
replies
10k
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Answer: Answer: What means Gaussian Kernel?
updated 2.1 years ago by 44k • written 9.3 years ago by ▴ 240
0
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0
replies
1.8k
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Comment: Comment: installing ACGH analysis packages in R
updated 2.1 years ago by 44k • written 9.3 years ago by ▴ 240
0
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0
replies
2.3k
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Comment: C: Read depths from 1000G exome sequencing are almost all zero.
9.3 years ago by eric.kern13 ▴ 240
3
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1
reply
3.1k
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Answer: A: Looking for experience
9.3 years ago by eric.kern13 ▴ 240
0
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2
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2.3k
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Comment: C: Read depths from 1000G exome sequencing are almost all zero.
9.3 years ago by eric.kern13 ▴ 240
2
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5
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2.3k
views
Read depths from 1000G exome sequencing are almost all zero.
next-gen-sequencing
updated 2.1 years ago by 44k • written 9.3 years ago by ▴ 240
0
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0
replies
1.9k
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Comment: Comment: Biojava HMM error
updated 2.1 years ago by 44k • written 9.3 years ago by ▴ 240
0
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4
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2.5k
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1000 genomes technical data: match exon capture probes to samples
next-gen
updated 2.1 years ago by 44k • written 9.3 years ago by ▴ 240
0
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0
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2.5k
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Answer: Answer: 1000 genomes technical data: match exon capture probes to samples
updated 2.1 years ago by 44k • written 9.3 years ago by ▴ 240
0
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0
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2.5k
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Comment: C: 1000 genomes technical data: match exon capture probes to samples
9.3 years ago by eric.kern13 ▴ 240
2
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1
reply
2.4k
views
+/- strand conventions for probe sequences
pcr sequence
updated 2.1 years ago by 44k • written 9.3 years ago by ▴ 240
0
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0
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5.7k
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Comment: C: Pysam cannot find index
9.3 years ago by eric.kern13 ▴ 240
0
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2
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5.7k
views
Comment: Comment: Pysam cannot find index
updated 2.1 years ago by 44k • written 9.3 years ago by ▴ 240
2
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6
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5.7k
views
Pysam cannot find index
Pysam samtools
updated 2.1 years ago by 44k • written 9.3 years ago by ▴ 240
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