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4
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Tool: MAGERI: a software tool for calling rare variants and detecting circulating tumor DNA from UMI-tagged high-throughput sequencing data
rare-variant resequencing umi ctDNA
updated 9 months ago by • 0 • written 7.5 years ago by 3.5k
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Answer: A: igBLAST query/options error
updated 3.9 years ago by 44k • written 9.9 years ago by 3.5k
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Comment: C: identification of level of gene expression related to first intron's cis- elemen
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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Comment: C: MIGEC: towards error-free profiling of immune repertoires
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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Answer: A: How to understand median 5 prime to 3 prime bias ratio from Picard?
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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Comment: C: MIGEC: towards error-free profiling of immune repertoires
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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11k
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Comment: C: MIGEC: towards error-free profiling of immune repertoires
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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1
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11k
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Comment: C: MIGEC: towards error-free profiling of immune repertoires
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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Answer: A: data from SRA against blast databases method.
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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Answer: A: appropriate statistics to test for differences in heterogeneous features betwee
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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Answer: A: What is the best programming language for NGS data analysis pipeline development
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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0
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Answer: A: Hypergeometric test for overlapped genes
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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1
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3.3k
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Answer: A: What is the RNA:Protein ratio for ONE gene over different RNA levels
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
3
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1
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20k
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Answer: A: Example publications for Individualized Medicine
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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Answer: A: Processed RNA-SEQ Datasets
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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1
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Answer: A: How Has Bioinformatics Improved Over Time?
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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Comment: C: How to test the robustness and the performance of a novel classification algorit
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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0
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Answer: A: In search of projects for collaboration.
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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1
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Answer: A: Making sense of Gene Ontology graph relations
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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1
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Comment: C: Software to determine whether genes are related to cancer
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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Comment: C: How to query for a specific motif upstream of each of the gene in a list?
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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Comment: C: How is a deletion with inserted bases simulated?
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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2.0k
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Answer: A: How is a deletion with inserted bases simulated?
updated 4.9 years ago by 44k • written 10.5 years ago by 3.5k
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0
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Answer: C: Microarray | RNA Seq | Methylation Arrays - Correlations?
updated 4.9 years ago by 44k • written 10.6 years ago by 3.5k
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0
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Comment: C: Oncofuse: Prediction Of Driver Gene Fusions From Ngs Data
updated 4.9 years ago by 44k • written 8.9 years ago by 3.5k
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1
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2.9k
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Answer: A: Protein Domains from fusions
updated 4.9 years ago by 44k • written 8.9 years ago by 3.5k
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0
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8.0k
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Comment: C: Oncofuse: Prediction Of Driver Gene Fusions From Ngs Data
updated 4.9 years ago by 44k • written 11.2 years ago by 3.5k
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0
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8.0k
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Comment: C: Oncofuse: Prediction Of Driver Gene Fusions From Ngs Data
updated 4.9 years ago by 44k • written 9.9 years ago by 3.5k
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1
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8.0k
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Comment: C: Oncofuse: Prediction Of Driver Gene Fusions From Ngs Data
updated 4.9 years ago by 44k • written 9.9 years ago by 3.5k
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1
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8.0k
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Comment: C: Oncofuse: Prediction Of Driver Gene Fusions From Ngs Data
updated 4.9 years ago by 44k • written 9.6 years ago by 3.5k
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1
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8.0k
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Comment: C: Oncofuse: Prediction Of Driver Gene Fusions From Ngs Data
updated 4.9 years ago by 44k • written 9.6 years ago by 3.5k
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0
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8.0k
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Comment: C: Oncofuse: Prediction Of Driver Gene Fusions From Ngs Data
updated 4.9 years ago by 44k • written 8.8 years ago by 3.5k
1
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1
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2.4k
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Comment: C: tophat-cuffdiff or tophat-cufflinks-cuffmerge-cuffdiff?
updated 5.0 years ago by 44k • written 9.0 years ago by 3.5k
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0
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3.2k
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Comment: C: Bioinformatics job to start.
updated 5.0 years ago by 44k • written 9.0 years ago by 3.5k
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1
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4.4k
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Comment: C: Annotating gene fusion predictions
updated 5.0 years ago by 44k • written 9.1 years ago by 3.5k
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1
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4.4k
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Answer: A: Annotating gene fusion predictions
updated 5.0 years ago by 44k • written 9.1 years ago by 3.5k
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1
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11k
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Comment: C: MIGEC: towards error-free profiling of immune repertoires
updated 5.0 years ago by 44k • written 9.3 years ago by 3.5k
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0
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4.3k
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Answer: A: Proteins without genes ? Is that even possible ?
updated 5.1 years ago by 44k • written 9.7 years ago by 3.5k
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0
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2.2k
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Answer: A: How To Search Disease Association For A List Of Gene Fusions?
updated 5.1 years ago by 44k • written 9.8 years ago by 3.5k
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0
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2.6k
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Answer: A: Methods to subset sequenced experiments to account for differences in read count
updated 5.1 years ago by 44k • written 10.4 years ago by 3.5k
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0
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2.1k
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Answer: A: Is there a good service for annotating transcripts?
updated 5.1 years ago by 44k • written 10.5 years ago by 3.5k
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1
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4.6k
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Answer: A: question about clustering of samples
updated 5.1 years ago by 44k • written 10.5 years ago by 3.5k
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0
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3.4k
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Answer: A: Which Aligner Would You Recommend For Transcriptome Assembly
updated 5.1 years ago by 44k • written 10.5 years ago by 3.5k
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0
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9.0k
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Comment: C: Number of aligned reads in exon, intron ...
updated 5.1 years ago by 44k • written 10.5 years ago by 3.5k
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0
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7.4k
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Answer: A: GO enrichment in non-model organism
updated 5.1 years ago by 44k • written 10.5 years ago by 3.5k
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0
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Answer: A: How to find a FASTA (CDS) of specified sequence?
updated 5.1 years ago by 44k • written 10.6 years ago by 3.5k
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0
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7.7k
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Answer: A: Rarefaction/Saturation Curve Based On Ngs Data
updated 5.2 years ago by 44k • written 9.9 years ago by 3.5k
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1
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4.8k
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Comment: C: MAGERI: a software tool for calling rare variants and detecting circulating tumo
5.8 years ago by mikhail.shugay 3.5k
2
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0
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16k
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Answer: A: Demultiplexing fastq files with dual barcodes
updated 5.9 years ago by 44k • written 9.6 years ago by 3.5k
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0
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3.1k
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Answer: A: T Cell Receptor Sequencing total reads/clone count vs unique clones
updated 6.2 years ago by 44k • written 8.7 years ago by 3.5k
353 results • Page 1 of 8
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