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Comment: C: Interpretation for lowfrevariant
7.1 years ago by Titus ▴ 910
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2.0k
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Comment: C: Interpretation for lowfrevariant
7.1 years ago by Titus ▴ 910
1
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1
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2.0k
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Comment: C: Interpretation for lowfrevariant
7.1 years ago by Titus ▴ 910
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2.1k
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Comment: C: Excluding reads for Coverage Calculation in given regions
7.1 years ago by Titus ▴ 910
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3.3k
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Comment: C: MAF file handling
7.1 years ago by Titus ▴ 910
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2.1k
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Comment: C: Excluding reads for Coverage Calculation in given regions
7.1 years ago by Titus ▴ 910
1
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1
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2.1k
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Comment: C: Excluding reads for Coverage Calculation in given regions
7.1 years ago by Titus ▴ 910
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2.2k
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Comment: C: HLA analysis using SNP2HLA
7.1 years ago by Titus ▴ 910
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2.0k
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Answer: C: 20 millions reads per sample for SNP
7.1 years ago by Titus ▴ 910
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1.6k
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Answer: C: SNP single end read
7.1 years ago by Titus ▴ 910
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831
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Comment: C: How to tackle homeologous region which calling SNP for Allotetraploid genome
7.1 years ago by Titus ▴ 910
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3.6k
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Comment: C: Why different rna-seq aligners need to be used for Ion Torrent data compared wit
7.1 years ago by Titus ▴ 910
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1
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5.0k
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Comment: C: Uniquly aligned reads by BWA-mem (MAPQ, and XA tag)
7.2 years ago by Titus ▴ 910
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1
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5.0k
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Comment: C: Uniquly aligned reads by BWA-mem (MAPQ, and XA tag)
7.2 years ago by Titus ▴ 910
1
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1
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5.0k
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Comment: C: Uniquly aligned reads by BWA-mem (MAPQ, and XA tag)
7.2 years ago by Titus ▴ 910
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2.7k
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Comment: C: Inconsistent Coverage on X chromosome between genders
7.2 years ago by Titus ▴ 910
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2.7k
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Comment: C: Inconsistent Coverage on X chromosome between genders
7.2 years ago by Titus ▴ 910
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1
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2.7k
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Comment: C: Inconsistent Coverage on X chromosome between genders
7.2 years ago by Titus ▴ 910
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2
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2.7k
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Comment: C: Inconsistent Coverage on X chromosome between genders
7.2 years ago by Titus ▴ 910
0
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1
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2.7k
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Comment: C: Inconsistent Coverage on X chromosome between genders
7.2 years ago by Titus ▴ 910
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1
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2.7k
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Comment: C: Inconsistent Coverage on X chromosome between genders
7.2 years ago by Titus ▴ 910
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2.0k
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Comment: C: visualization of identified SSRs
7.2 years ago by Titus ▴ 910
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1.4k
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Comment: C: De novo sequencing?
7.2 years ago by Titus ▴ 910
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7.2k
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Comment: C: Exon coordinates and sequence
7.2 years ago by Titus ▴ 910
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1
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7.2k
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Comment: C: Exon coordinates and sequence
7.2 years ago by Titus ▴ 910
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3
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1.5k
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Forum: Looking for advice application devellopment
next-gen
updated 21 months ago by 44k • written 7.2 years ago by ▴ 910
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1.5k
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Comment: C: Looking for advice application devellopment
7.2 years ago by Titus ▴ 910
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1
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4.1k
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Comment: C: Annotation of XHMM VCF file (CNV analysis)
7.3 years ago by Titus ▴ 910
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1
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4.1k
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Comment: C: Annotation of XHMM VCF file (CNV analysis)
7.3 years ago by Titus ▴ 910
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1
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4.1k
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Comment: C: Annotation of XHMM VCF file (CNV analysis)
7.3 years ago by Titus ▴ 910
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1
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4.1k
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Comment: C: Annotation of XHMM VCF file (CNV analysis)
7.3 years ago by Titus ▴ 910
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1
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4.1k
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Comment: C: Annotation of XHMM VCF file (CNV analysis)
7.3 years ago by Titus ▴ 910
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1
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4.1k
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Comment: C: Annotation of XHMM VCF file (CNV analysis)
7.3 years ago by Titus ▴ 910
2
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2.0k
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Comment: C: Tools for Copy Number Variation analysis from ion Proton data.
7.3 years ago by Titus ▴ 910
1
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1
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2.0k
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Comment: C: Tools for Copy Number Variation analysis from ion Proton data.
7.3 years ago by Titus ▴ 910
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3.5k
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Comment: C: Variant Calling in Low-Complexity Regions
7.4 years ago by Titus ▴ 910
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1
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3.5k
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Comment: C: Variant Calling in Low-Complexity Regions
7.4 years ago by Titus ▴ 910
1
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1
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2.6k
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Comment: C: CDS FASTA file as Reference sequence for Ion Torrent
7.4 years ago by Titus ▴ 910
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1
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2.7k
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Comment: C: Looking for wig base coverage file for hg19
7.4 years ago by Titus ▴ 910
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0
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3.7k
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Comment: C: how to get exact break point in COSMIC fusion gene?
7.4 years ago by Titus ▴ 910
1
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0
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2.7k
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Comment: C: Locate short DNA sequence from fasta file
7.4 years ago by Titus ▴ 910
3
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2
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2.4k
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Comment: C: BRCA1 and BRCA2 database's for NGS diagnostics purposes
7.4 years ago by Titus ▴ 910
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0
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2.8k
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Comment: C: How to reduce cross mapping alignments with paired-end reads ?
7.5 years ago by Titus ▴ 910
0
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1
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2.8k
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Comment: C: How to reduce false positive whan aligning paired-end reads ?
7.5 years ago by Titus ▴ 910
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2.8k
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Comment: C: How to reduce false positive whan aligning paired-end reads ?
7.5 years ago by Titus ▴ 910
0
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0
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2.8k
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Comment: C: How to reduce false positive whan aligning paired-end reads ?
7.5 years ago by Titus ▴ 910
3
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3.1k
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Comment: C: Which tool is recommended for detecting CNVs in whole exome sequencing?
7.5 years ago by Titus ▴ 910
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1
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4.0k
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Comment: C: Aligning short sequences to fastq
7.5 years ago by Titus ▴ 910
1
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4.3k
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Comment: C: Structural Variant annotation
7.5 years ago by Titus ▴ 910
0
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0
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2.0k
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Comment: C: RUM aligner - perl precedence error
7.5 years ago by Titus ▴ 910
245 results • Page 3 of 5
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