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Downloading BED files for Roche Oncology Kits
Bed_file
updated 2.3 years ago by ★ 1.8k • written 2.3 years ago by ▴ 100
2
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4
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1.4k
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adding Gene Name to my bed file
name annotation gene bed
21 months ago by manojkumarbioinfo ▴ 100
2
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0
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1.4k
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Answer: Answer: adding Gene Name to my bed file
21 months ago by manojkumarbioinfo ▴ 100
0
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1
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922
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Comment: Comment: CNV kit merge all my gene names together
2.3 years ago by manojkumarbioinfo ▴ 100
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3
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922
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CNV kit merge all my gene names together
CNV CNVkit
updated 2.3 years ago by ▴ 830 • written 2.3 years ago by ▴ 100
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0
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2.5k
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Comment: Comment: Extract the DP and AD from VCF file along with the chromosome postion and alter
2.4 years ago by manojkumarbioinfo ▴ 100
3
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3
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2.5k
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Extract the DP and AD from VCF file along with the chromosome postion and alteration
VCF
updated 2.4 years ago by 161k • written 2.4 years ago by ▴ 100
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0
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2.5k
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Answer: Answer: Extract the DP and AD from VCF file along with the chromosome postion and alter
2.4 years ago by manojkumarbioinfo ▴ 100
3
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4
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1.2k
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Extract the DP from VCF file along with the chromosome postion and alteration
DP vcf
2.5 years ago by manojkumarbioinfo ▴ 100
1
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0
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1.2k
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Answer: Answer: Extract the DP from VCF file along with the chromosome postion and alteration
2.5 years ago by manojkumarbioinfo ▴ 100
1
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0
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1.2k
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Comment: Comment: Extract the DP from VCF file along with the chromosome postion and alteration
2.5 years ago by manojkumarbioinfo ▴ 100
0
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0
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1.2k
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Comment: Comment: Extract the DP from VCF file along with the chromosome postion and alteration
2.5 years ago by manojkumarbioinfo ▴ 100
0
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0
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1.4k
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Comment: Comment: adding Gene Name to my bed file
2.5 years ago by manojkumarbioinfo ▴ 100
1
vote
1
reply
678
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Whole Exome sequenincg Variant Priortization
NGS WES WGS Variant Priortization
updated 3.2 years ago by • 0 • written 3.2 years ago by ▴ 100
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0
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577
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Extracting the Predicted Reults of Neural network in R
R Neural-network NGS expression
3.3 years ago by manojkumarbioinfo ▴ 100
3
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1
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2.5k
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Answer: A: How to remove sequence reads contains more than 1 X from multifasta file?
4.0 years ago by manojkumarbioinfo ▴ 100
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0
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2.7k
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Comment: C: Regarding Depth coverage
updated 4.4 years ago by 43k • written 8.3 years ago by ▴ 100
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1
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2.7k
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Comment: C: Regarding Depth coverage
updated 4.4 years ago by 43k • written 8.3 years ago by ▴ 100
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4.2k
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Comment: C: Error, fewer reads in file specified with -2 than in file specified with -1
4.4 years ago by manojkumarbioinfo ▴ 100
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0
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4.0k
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Comment: C: Error with Bowtie 2
4.4 years ago by manojkumarbioinfo ▴ 100
2
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3
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4.2k
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Error, fewer reads in file specified with -2 than in file specified with -1
NGS Bowtie2 sequencing WGS
updated 4.4 years ago by 35k • written 4.4 years ago by ▴ 100
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2
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3.0k
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Comment: C: Extracting Bar code From Fastq file
updated 5.7 years ago by 141k • written 5.7 years ago by ▴ 100
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5
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3.0k
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Extracting Bar code From Fastq file
next-gen Assembly sequencing
5.7 years ago by manojkumarbioinfo ▴ 100
0
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0
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1.7k
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Comment: C: Error while aligning the sequence using Novoalign
5.7 years ago by manojkumarbioinfo ▴ 100
1
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3
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1.7k
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Error while aligning the sequence using Novoalign
next-gen NGS alignment
updated 5.7 years ago by ▴ 70 • written 7.0 years ago by ▴ 100
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0
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4.0k
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Comment: C: Calculate the Quality of Bases
6.7 years ago by manojkumarbioinfo ▴ 100
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1
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4.0k
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Comment: C: Calculate the Quality of Bases
6.7 years ago by manojkumarbioinfo ▴ 100
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1
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4.0k
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Comment: C: Calculate the Quality of Bases
6.7 years ago by manojkumarbioinfo ▴ 100
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2
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4.0k
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Comment: C: Calculate the Quality of Bases
6.7 years ago by manojkumarbioinfo ▴ 100
0
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1
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4.0k
views
Comment: C: Calculate the Quality of Bases
6.7 years ago by manojkumarbioinfo ▴ 100
0
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12
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4.0k
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Calculate the Quality of Bases
next-gen alignment sequencing
updated 6.7 years ago by ▴ 660 • written 6.7 years ago by ▴ 100
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0
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1.8k
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Comment: C: SVM based VCF filter
7.2 years ago by manojkumarbioinfo ▴ 100
0
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4
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1.8k
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SVM based VCF filter
NGS SVM VCF
updated 7.3 years ago by ★ 1.9k • written 7.3 years ago by ▴ 100
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0
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1.8k
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Comment: C: SVM based VCF filter
7.3 years ago by manojkumarbioinfo ▴ 100
0
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0
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1.9k
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Comment: C: SVM based Filtering For NGS data
7.3 years ago by manojkumarbioinfo ▴ 100
0
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2
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1.9k
views
SVM based Filtering For NGS data
next-gen SVM Filtering Variant
updated 7.3 years ago by ★ 2.7k • written 7.3 years ago by ▴ 100
3
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2
replies
3.1k
views
Comparing VCF with dbsnp
next-gen dbsnp VCF RTG
updated 12 months ago by • 0 • written 8.1 years ago by ▴ 100
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0
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2.2k
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Comment: C: Simulation Tools To Generate Next-Generation Sequencing Reads along with their
7.8 years ago by manojkumarbioinfo ▴ 100
3
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3
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2.2k
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Simulation Tools To Generate Next-Generation Sequencing Reads along with their VCF
VCF NGS sequencing
7.8 years ago by manojkumarbioinfo ▴ 100
0
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0
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2.3k
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Comment: C: VCF - Annotation
7.9 years ago by manojkumarbioinfo ▴ 100
1
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2
replies
2.3k
views
VCF - Annotation
sequencing VCF Annotation NGS
updated 7.9 years ago by 23k • written 7.9 years ago by ▴ 100
1
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3
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3.7k
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VCF - compare
next-gen sequencing
updated 8.0 years ago by 7.3k • written 8.0 years ago by ▴ 100
0
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1
reply
3.8k
views
Freebayes Variant calling
Freebayes NGS
updated 8.1 years ago by ▴ 110 • written 8.2 years ago by ▴ 100
3
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2
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7.7k
views
Answer: A: Difference Between GATK, Freebayes and SAMtools mpileup
8.1 years ago by manojkumarbioinfo ▴ 100
7
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7
replies
7.7k
views
Difference Between GATK, Freebayes and SAMtools mpileup
NGS Variant Caller
8.1 years ago by manojkumarbioinfo ▴ 100
1
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4
replies
2.7k
views
Regarding Depth coverage
NGS genome
updated 21 months ago by 43k • written 8.3 years ago by ▴ 100
5
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1
reply
6.1k
views
Incompatible contigs No overlapping contigs found.
NGS sequencing
updated 20 months ago by 43k • written 8.4 years ago by ▴ 100
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