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Downloading BED files for Roche Oncology Kits
Bed_file
updated 2.9 years ago by ★ 1.8k • written 2.9 years ago by ▴ 100
2
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4
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1.6k
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adding Gene Name to my bed file
name annotation gene bed
2.4 years ago by manojkumarbioinfo ▴ 100
2
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0
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1.6k
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Answer: Answer: adding Gene Name to my bed file
2.4 years ago by manojkumarbioinfo ▴ 100
0
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1
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1.1k
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Comment: Comment: CNV kit merge all my gene names together
2.9 years ago by manojkumarbioinfo ▴ 100
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3
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1.1k
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CNV kit merge all my gene names together
CNV CNVkit
updated 2.9 years ago by ▴ 830 • written 2.9 years ago by ▴ 100
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0
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2.9k
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Comment: Comment: Extract the DP and AD from VCF file along with the chromosome postion and alter
3.0 years ago by manojkumarbioinfo ▴ 100
3
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3
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2.9k
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Extract the DP and AD from VCF file along with the chromosome postion and alteration
VCF
updated 3.0 years ago by 164k • written 3.0 years ago by ▴ 100
1
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0
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2.9k
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Answer: Answer: Extract the DP and AD from VCF file along with the chromosome postion and alter
3.0 years ago by manojkumarbioinfo ▴ 100
3
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4
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1.3k
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Extract the DP from VCF file along with the chromosome postion and alteration
DP vcf
3.1 years ago by manojkumarbioinfo ▴ 100
1
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0
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1.3k
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Answer: Answer: Extract the DP from VCF file along with the chromosome postion and alteration
3.1 years ago by manojkumarbioinfo ▴ 100
1
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0
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1.3k
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Comment: Comment: Extract the DP from VCF file along with the chromosome postion and alteration
3.1 years ago by manojkumarbioinfo ▴ 100
0
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0
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1.3k
views
Comment: Comment: Extract the DP from VCF file along with the chromosome postion and alteration
3.1 years ago by manojkumarbioinfo ▴ 100
0
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0
replies
1.6k
views
Comment: Comment: adding Gene Name to my bed file
3.1 years ago by manojkumarbioinfo ▴ 100
1
vote
1
reply
738
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Whole Exome sequenincg Variant Priortization
NGS WES WGS Variant Priortization
updated 3.8 years ago by • 0 • written 3.8 years ago by ▴ 100
0
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0
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654
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Extracting the Predicted Reults of Neural network in R
R Neural-network NGS expression
3.8 years ago by manojkumarbioinfo ▴ 100
3
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1
reply
2.9k
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Answer: A: How to remove sequence reads contains more than 1 X from multifasta file?
4.5 years ago by manojkumarbioinfo ▴ 100
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0
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2.9k
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Comment: C: Regarding Depth coverage
updated 4.9 years ago by 44k • written 8.9 years ago by ▴ 100
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1
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2.9k
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Comment: C: Regarding Depth coverage
updated 4.9 years ago by 44k • written 8.9 years ago by ▴ 100
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0
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4.4k
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Comment: C: Error, fewer reads in file specified with -2 than in file specified with -1
5.0 years ago by manojkumarbioinfo ▴ 100
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0
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4.3k
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Comment: C: Error with Bowtie 2
5.0 years ago by manojkumarbioinfo ▴ 100
2
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3
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4.4k
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Error, fewer reads in file specified with -2 than in file specified with -1
NGS Bowtie2 sequencing WGS
updated 5.0 years ago by 35k • written 5.0 years ago by ▴ 100
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2
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3.1k
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Comment: C: Extracting Bar code From Fastq file
updated 6.2 years ago by 147k • written 6.2 years ago by ▴ 100
1
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5
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3.1k
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Extracting Bar code From Fastq file
next-gen Assembly sequencing
6.2 years ago by manojkumarbioinfo ▴ 100
0
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0
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1.9k
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Comment: C: Error while aligning the sequence using Novoalign
6.2 years ago by manojkumarbioinfo ▴ 100
1
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3
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1.9k
views
Error while aligning the sequence using Novoalign
next-gen NGS alignment
updated 6.2 years ago by ▴ 70 • written 7.5 years ago by ▴ 100
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0
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4.6k
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Comment: C: Calculate the Quality of Bases
7.2 years ago by manojkumarbioinfo ▴ 100
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1
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4.6k
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Comment: C: Calculate the Quality of Bases
7.2 years ago by manojkumarbioinfo ▴ 100
0
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1
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4.6k
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Comment: C: Calculate the Quality of Bases
7.2 years ago by manojkumarbioinfo ▴ 100
0
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2
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4.6k
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Comment: C: Calculate the Quality of Bases
7.2 years ago by manojkumarbioinfo ▴ 100
0
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1
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4.6k
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Comment: C: Calculate the Quality of Bases
7.2 years ago by manojkumarbioinfo ▴ 100
0
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12
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4.6k
views
Calculate the Quality of Bases
next-gen alignment sequencing
updated 7.2 years ago by ▴ 670 • written 7.2 years ago by ▴ 100
0
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0
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1.9k
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Comment: C: SVM based VCF filter
7.8 years ago by manojkumarbioinfo ▴ 100
0
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4
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1.9k
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SVM based VCF filter
NGS SVM VCF
updated 7.9 years ago by ★ 1.9k • written 7.9 years ago by ▴ 100
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0
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1.9k
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Comment: C: SVM based VCF filter
7.9 years ago by manojkumarbioinfo ▴ 100
0
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0
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2.1k
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Comment: C: SVM based Filtering For NGS data
7.9 years ago by manojkumarbioinfo ▴ 100
0
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2
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2.1k
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SVM based Filtering For NGS data
next-gen SVM Filtering Variant
updated 7.9 years ago by ★ 2.7k • written 7.9 years ago by ▴ 100
3
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2
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3.3k
views
Comparing VCF with dbsnp
next-gen dbsnp VCF RTG
updated 19 months ago by • 0 • written 8.7 years ago by ▴ 100
0
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0
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2.3k
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Comment: C: Simulation Tools To Generate Next-Generation Sequencing Reads along with their
8.4 years ago by manojkumarbioinfo ▴ 100
3
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3
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2.3k
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Simulation Tools To Generate Next-Generation Sequencing Reads along with their VCF
VCF NGS sequencing
8.4 years ago by manojkumarbioinfo ▴ 100
0
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0
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2.4k
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Comment: C: VCF - Annotation
8.4 years ago by manojkumarbioinfo ▴ 100
1
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2
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2.4k
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VCF - Annotation
sequencing VCF Annotation NGS
updated 8.4 years ago by 24k • written 8.4 years ago by ▴ 100
1
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3
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3.9k
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VCF - compare
next-gen sequencing
updated 8.6 years ago by 7.3k • written 8.6 years ago by ▴ 100
0
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1
reply
3.9k
views
Freebayes Variant calling
Freebayes NGS
updated 8.7 years ago by ▴ 110 • written 8.7 years ago by ▴ 100
7
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7
replies
8.1k
views
Difference Between GATK, Freebayes and SAMtools mpileup
NGS Variant Caller
8.7 years ago by manojkumarbioinfo ▴ 100
3
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2
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8.1k
views
Answer: A: Difference Between GATK, Freebayes and SAMtools mpileup
8.7 years ago by manojkumarbioinfo ▴ 100
1
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4
replies
2.9k
views
Regarding Depth coverage
NGS genome
updated 2.3 years ago by 44k • written 8.9 years ago by ▴ 100
5
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1
reply
6.2k
views
Incompatible contigs No overlapping contigs found.
NGS sequencing
updated 2.3 years ago by 44k • written 9.0 years ago by ▴ 100
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