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Comment: C: 4C-seq analysis using FourCSeq R package
8.7 years ago by User 59 13k
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3.0k
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Comment: C: RAPIDR(NIPT analysis ) report error
8.7 years ago by User 59 13k
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2
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3.0k
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Comment: C: RAPIDR(NIPT analysis ) report error
8.8 years ago by User 59 13k
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1
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3.0k
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Comment: C: RAPIDR(NIPT analysis ) report error
8.8 years ago by User 59 13k
0
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3.0k
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Answer: C: RAPIDR(NIPT analysis ) report error
8.8 years ago by User 59 13k
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2.5k
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Answer: A: Is there an online repository for denovo assemblers?
8.8 years ago by User 59 13k
2
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2.5k
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Comment: C: how many read per sample give me good coverage for soybean rna sequensing with 1
8.8 years ago by User 59 13k
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1
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3.1k
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Comment: C: How to find a better performance NIPT analysis scripts ?
8.8 years ago by User 59 13k
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1
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3.8k
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Answer: A: Reason for Freebayes Calling Multi-base Variants
8.8 years ago by User 59 13k
2
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1
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39k
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Comment: C: Ensembl ID to Gene Symbol
8.8 years ago by User 59 13k
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1
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3.0k
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Comment: C: What is the correct way to cite a technology like ABI Solid Sequencing?
8.8 years ago by User 59 13k
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4.7k
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Comment: C: Unzipping bz2 files
8.8 years ago by User 59 13k
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2.1k
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Answer: A: Is this SNP inside an intron or extron, or neither?
8.8 years ago by User 59 13k
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1
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4.7k
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Comment: C: Unzipping bz2 files
8.8 years ago by User 59 13k
2
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1
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3.3k
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Answer: A: CpG-SNPs for newbies
8.9 years ago by User 59 13k
1
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0
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2.4k
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Answer: A: Cross-species contamination in NGS data
8.9 years ago by User 59 13k
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1
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2.3k
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Comment: C: Variant annotation tool
8.9 years ago by User 59 13k
1
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1
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25k
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Comment: C: Cleaning RNA-Seq data from rRNA
8.9 years ago by User 59 13k
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2.5k
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Comment: C: Are these reads all PCR replicates ?
9.0 years ago by User 59 13k
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3.0k
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Comment: C: Velvet Assembly Online
9.0 years ago by User 59 13k
3
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1
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12k
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Comment: C: Bimodal GC content
9.0 years ago by User 59 13k
1
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1
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3.3k
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Comment: C: Is it ok to map RNA-seq reads on prokaryotic reference genome with bowtie2 ?
9.0 years ago by User 59 13k
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0
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2.9k
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Answer: A: Doubts in Agilent Sure select DNA design
9.0 years ago by User 59 13k
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0
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2.9k
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Comment: C: Agilent SureSelect design miss some target regions
9.0 years ago by User 59 13k
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2.4k
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Answer: C: Illumina small RNAseq analysis pipeline?
9.0 years ago by User 59 13k
1
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0
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2.9k
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Answer: A: Agilent SureSelect design miss some target regions
9.1 years ago by User 59 13k
0
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1
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3.9k
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Comment: C: PacBio sequences, proovread correction with Illumina HiSeq reads
9.1 years ago by User 59 13k
2
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1
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2.6k
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Answer: C: Coverage depth and breadth after recaliberation
9.1 years ago by User 59 13k
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0
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2.6k
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Comment: C: SOLiD reads unreadable to Bowtie after unpacking from .sra archive
9.1 years ago by User 59 13k
1
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0
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2.6k
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Comment: A: SOLiD reads unreadable to Bowtie after unpacking from .sra archive
9.1 years ago by User 59 13k
0
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0
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2.4k
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Comment: C: Low quality bases at the starts of HiSeq 2 x 100bp reads
9.1 years ago by User 59 13k
0
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1
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6.4k
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Comment: C: Error: Could not find Bowtie 2 index files (p.*.bt2)
9.1 years ago by User 59 13k
0
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1
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4.9k
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Comment: C: How to use BBMap for aligning a set of .fastq files?
9.1 years ago by User 59 13k
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1
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3.0k
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Comment: C: I need help in this
9.1 years ago by User 59 13k
1
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0
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5.3k
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Comment: C: different between CEL and CHIP files in microarray
9.2 years ago by User 59 13k
0
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0
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5.4k
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Comment: C: Creating a Venn Diagram from Microarray Data
9.2 years ago by User 59 13k
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1
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3.1k
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Comment: C: Allele frequencies in pedigrees
9.2 years ago by User 59 13k
3
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1
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3.1k
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Comment: C: Allele frequencies in pedigrees
9.2 years ago by User 59 13k
1
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1
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5.8k
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Comment: C: Lack of consensus between NGS & Sanger sequencing on indels/mutations
9.2 years ago by User 59 13k
3
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0
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4.2k
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Comment: C: VCF file alignment to the reference genome
9.3 years ago by User 59 13k
2
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0
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2.0k
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Answer: C: Restrict ANNOVAR annotation to a list of genes.
9.3 years ago by User 59 13k
3
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2
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4.2k
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Answer: A: VCF file alignment to the reference genome
9.3 years ago by User 59 13k
1
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0
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2.5k
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Comment: C: checking many somatic mutations in IGV
9.3 years ago by User 59 13k
1
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0
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3.9k
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Answer: A: Database for plant ploidy
9.3 years ago by User 59 13k
0
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0
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9.5k
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Comment: C: How many reads should I expect for paired end reads when coverage = 30 million?
9.3 years ago by User 59 13k
7
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0
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7.2k
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Answer: A: Why 50bp Illumina run produces 51bp long sequencs?
9.3 years ago by User 59 13k
0
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0
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1.9k
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Comment: C: Windows IGV control through port / automatic taking pictures / manually inspect
9.3 years ago by User 59 13k
0
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1
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5.1k
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Comment: C: Should I use Illumina or Ion Torrent for producing data intended for genome rese
9.3 years ago by User 59 13k
3
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2
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8.5k
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Answer: Answer: bwa error: paired reads have different names
updated 2.4 years ago by 44k • written 9.4 years ago by 13k
3
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1
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4.1k
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Answer: Answer: Illumina hiseq and pacbio isoseq data on same set of samples- combined analysis
updated 2.4 years ago by 44k • written 9.4 years ago by 13k
658 results • Page 3 of 14
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