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Answer: A: Single cell Expression Analysis
5.8 years ago by swbarnes2 15k
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Comment: C: How to identify 100ish deletion from NGS data
5.8 years ago by swbarnes2 15k
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Comment: C: How to identify 100ish deletion from NGS data
5.8 years ago by swbarnes2 15k
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Answer: A: Sequencing index information from BAM
5.8 years ago by swbarnes2 15k
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Comment: C: Script to download fasta seqeuences for FGF1 to FGF12
5.8 years ago by swbarnes2 15k
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1.8k
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Answer: A: How to identify 100ish deletion from NGS data
5.8 years ago by swbarnes2 15k
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1.5k
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Answer: A: Script to download fasta seqeuences for FGF1 to FGF12
5.8 years ago by swbarnes2 15k
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3.9k
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Comment: C: Cellranger data to Monocle Pseudotime
5.8 years ago by swbarnes2 15k
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1.8k
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Comment: C: Can a statistically associated mutation by Fisher's Exact Test, really not be as
5.8 years ago by swbarnes2 15k
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Comment: C: Combining datasets from different sequencing platforms
5.8 years ago by swbarnes2 15k
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1.7k
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Comment: C: sequence in bam file looks weird
5.8 years ago by swbarnes2 15k
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Answer: A: getting 0 counts using hisat2 and feature_count pipeline
5.8 years ago by swbarnes2 15k
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Answer: A: software of single-cell RNA-seq from fastq or fasta
5.8 years ago by swbarnes2 15k
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Comment: C: sequence in bam file looks weird
5.8 years ago by swbarnes2 15k
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Answer: A: How to analyze the RNAseq paired samples with DESeq2?
5.8 years ago by swbarnes2 15k
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Comment: C: Splitting BAM file from paired end into forward and reverse strands?
5.9 years ago by swbarnes2 15k
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Answer: A: Deseq2 multiple variables!
5.9 years ago by swbarnes2 15k
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Comment: C: Missing SNPs in sequencing.com from BAM file
5.9 years ago by swbarnes2 15k
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4.3k
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Comment: C: Missing SNPs in sequencing.com from BAM file
5.9 years ago by swbarnes2 15k
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Answer: A: Aligning, Sorting and Converting to bam at the same command - possible?
5.9 years ago by swbarnes2 15k
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Answer: A: Any user friendly way to find rare mutations in whole genome raw?
5.9 years ago by swbarnes2 15k
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Comment: C: How to remove duplicate reads / create consensus reads based on umi tags in 2nd
5.9 years ago by swbarnes2 15k
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Answer: A: Finding a sequence in a fasta file
updated 5.9 years ago by 45k • written 11.5 years ago by 15k
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Comment: C: Can'T Find Indels With Samtools (Onyly Get Snps)
updated 5.9 years ago by 45k • written 11.5 years ago by 15k
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Answer: A: RS SNP's to Protein Change name please
5.9 years ago by swbarnes2 15k
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Comment: C: Alignment using BWA tool
5.9 years ago by swbarnes2 15k
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Answer: A: Alignment using BWA tool
5.9 years ago by swbarnes2 15k
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8.0k
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Comment: C: Salvage barcode undetermined reads from Illumina HiSeq 2500 2 x 100 bp pair-ende
updated 5.9 years ago by 45k • written 9.8 years ago by 15k
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Comment: C: Alignment using BWA tool
5.9 years ago by swbarnes2 15k
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11k
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Comment: C: Most effective way to merge individual VCF files into VCF files merged by chromo
updated 5.9 years ago by 45k • written 11.5 years ago by 15k
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Answer: A: variant calls which are important
updated 5.9 years ago by 45k • written 11.6 years ago by 15k
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3.6k
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Answer: Answer: Header In Mpileup Output File
updated 4.2 years ago by 45k • written 11.6 years ago by 15k
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2.9k
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Comment: C: Identifying mutations from Paired-End Sequencing data
updated 5.9 years ago by 45k • written 11.6 years ago by 15k
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Comment: C: Can anyone suggest me the recent and best pipeline for RNA-Seq data analysis
5.9 years ago by swbarnes2 15k
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986
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Comment: C: Paired end data with R1 demultiplexed but not R2
5.9 years ago by swbarnes2 15k
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Comment: C: Extract all BAM reads that intersect a given region using the BAI index
5.9 years ago by swbarnes2 15k
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1.7k
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Answer: A: Extract all BAM reads that intersect a given region using the BAI index
5.9 years ago by swbarnes2 15k
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Answer: A: converting RF strand-specific mRNA sequencing data to FR stand-specific
5.9 years ago by swbarnes2 15k
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4.9k
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Answer: A: Bulk RNA-Seq pipeline suggestion incorporating UMIs
5.9 years ago by swbarnes2 15k
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1
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5.9k
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Comment: C: Error when running cellranger mkref single nuclei RNA-Seq
5.9 years ago by swbarnes2 15k
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5.7k
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Answer: A: Please Help Me Check My Workflow For Paired-End Sequencing
updated 5.9 years ago by 45k • written 12.6 years ago by 15k
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Comment: C: What is the Variance means in PCA plot ?
5.9 years ago by swbarnes2 15k
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2.2k
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Answer: A: What is the Variance means in PCA plot ?
5.9 years ago by swbarnes2 15k
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Comment: C: Error in the creation of a consensus sequence from pileup
updated 6.0 years ago by 45k • written 9.9 years ago by 15k
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Answer: A: There is some way to split a FastQ file by chromosome?
6.0 years ago by swbarnes2 15k
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3.6k
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Comment: C: Is there a way to convert a FASTQ file to FASTA file?
6.0 years ago by swbarnes2 15k
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3.6k
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Answer: A: Is there a way to convert a FASTQ file to FASTA file?
6.0 years ago by swbarnes2 15k
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852
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Answer: A: re-assembling the reference
6.0 years ago by swbarnes2 15k
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Comment: C: RNA-seq healthy sample
6.0 years ago by swbarnes2 15k
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Answer: A: Can cell ranger count take a folder of only .fastq.gz as input?
6.0 years ago by swbarnes2 15k
2,124 results • Page 26 of 43
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