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Comment: C: How to tell bloodtype from SNPs data?
3.1 years ago by eric.kern13 ▴ 240
0
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1
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13k
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Comment: A: Unable to install XLconnect package in R studio version 3.2.1
updated 4.4 years ago by 43k • written 8.7 years ago by ▴ 240
4
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1
reply
12k
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Answer: A: Downloading a Small VCF File
updated 4.4 years ago by 43k • written 8.7 years ago by ▴ 240
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1
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21k
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Comment: C: Using Seurat 3 Data for Pseudotime Analysis in Monocle 3
4.5 years ago by eric.kern13 ▴ 240
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0
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1.3k
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Comment: C: Help setting up lncRNA-screen from github
5.3 years ago by eric.kern13 ▴ 240
8
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0
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56k
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Comment: C: How To Write Data In A Granges Object To A Bed File.
5.5 years ago by eric.kern13 ▴ 240
0
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0
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8.4k
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Answer: A: Adapter/Linker/Primer Sequence Database?
5.7 years ago by eric.kern13 ▴ 240
2
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2
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2.7k
views
Mappability Scores from bigWigAverageOverBed all zero
sequencing
updated 19 months ago by 43k • written 8.6 years ago by ▴ 240
1
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0
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2.1k
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Answer: A: Overdispersion for single cell RNA seq experiments
6.2 years ago by eric.kern13 ▴ 240
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0
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3.2k
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Comment: C: Question about dbSNP rs #s
6.5 years ago by eric.kern13 ▴ 240
0
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1
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26k
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Comment: C: Duplicated Reads In Rna-Seq Experiment
6.7 years ago by eric.kern13 ▴ 240
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0
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53k
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Comment: C: Should We Remove Duplicated Reads In Rna-Seq ?
6.7 years ago by eric.kern13 ▴ 240
0
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1
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2.1k
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What happens during seed stitching when STAR initially gets the wrong MMP?
rna-seq STAR
updated 6.9 years ago by 5.7k • written 6.9 years ago by ▴ 240
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0
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1.9k
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Comment: C: Retrieve all genes under a mammalian phenotype ontology term
7.0 years ago by eric.kern13 ▴ 240
2
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4
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1.9k
views
Retrieve all genes under a mammalian phenotype ontology term
R GO Mammalian Phenotype Ontology Biomart
updated 7.0 years ago by ★ 2.0k • written 7.0 years ago by ▴ 240
0
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0
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1.9k
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Comment: C: Retrieve all genes under a mammalian phenotype ontology term
7.0 years ago by eric.kern13 ▴ 240
0
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0
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3.9k
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Comment: C: cell surface receptor genes
7.5 years ago by eric.kern13 ▴ 240
1
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1
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3.7k
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Interpreting ANNOVAR allele frequency output
sequencing genome
7.5 years ago by eric.kern13 ▴ 240
1
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0
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3.7k
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Answer: A: Interpreting ANNOVAR allele frequency output
7.5 years ago by eric.kern13 ▴ 240
0
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0
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2.3k
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Comment: C: EdgeR or Ttest/ANOVA for non normal RNAseq data?
8.0 years ago by eric.kern13 ▴ 240
0
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0
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5.1k
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Comment: C: Can someone help me with imputation of missing SNPs using beagle 4?
8.0 years ago by eric.kern13 ▴ 240
0
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0
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2.0k
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Answer: Answer: Comparing results from ADMIXTURE and EIGENSTRAT
updated 19 months ago by 43k • written 8.5 years ago by ▴ 240
1
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0
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12k
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Comment: C: Should I use the p-value or q-value for pathway analysis in DAVID?
8.6 years ago by eric.kern13 ▴ 240
1
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0
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2.7k
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Comment: C: Mappability Scores from bigWigAverageOverBed all zero
8.6 years ago by eric.kern13 ▴ 240
1
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1
reply
2.7k
views
Answer: Answer: Mappability Scores from bigWigAverageOverBed all zero
updated 19 months ago by 43k • written 8.6 years ago by ▴ 240
2
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0
replies
9.3k
views
Answer: Answer: What means Gaussian Kernel?
updated 18 months ago by 43k • written 8.7 years ago by ▴ 240
0
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0
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1.7k
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Comment: Comment: installing ACGH analysis packages in R
updated 18 months ago by 43k • written 8.7 years ago by ▴ 240
0
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0
replies
2.1k
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Comment: C: Read depths from 1000G exome sequencing are almost all zero.
8.7 years ago by eric.kern13 ▴ 240
3
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1
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2.9k
views
Answer: A: Looking for experience
8.7 years ago by eric.kern13 ▴ 240
0
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2
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2.1k
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Comment: C: Read depths from 1000G exome sequencing are almost all zero.
8.7 years ago by eric.kern13 ▴ 240
2
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5
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2.1k
views
Read depths from 1000G exome sequencing are almost all zero.
next-gen-sequencing
updated 18 months ago by 43k • written 8.7 years ago by ▴ 240
0
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0
replies
1.8k
views
Comment: Comment: Biojava HMM error
updated 18 months ago by 43k • written 8.7 years ago by ▴ 240
0
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0
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2.4k
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Answer: Answer: 1000 genomes technical data: match exon capture probes to samples
updated 18 months ago by 43k • written 8.7 years ago by ▴ 240
0
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4
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2.4k
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1000 genomes technical data: match exon capture probes to samples
next-gen
updated 18 months ago by 43k • written 8.7 years ago by ▴ 240
0
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0
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2.4k
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Comment: C: 1000 genomes technical data: match exon capture probes to samples
8.7 years ago by eric.kern13 ▴ 240
2
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1
reply
2.3k
views
+/- strand conventions for probe sequences
pcr sequence
updated 18 months ago by 43k • written 8.7 years ago by ▴ 240
0
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0
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5.5k
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Comment: C: Pysam cannot find index
8.7 years ago by eric.kern13 ▴ 240
0
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2
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5.5k
views
Comment: Comment: Pysam cannot find index
updated 18 months ago by 43k • written 8.7 years ago by ▴ 240
2
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6
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5.5k
views
Pysam cannot find index
Pysam samtools
updated 18 months ago by 43k • written 8.7 years ago by ▴ 240
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