SRX825337 GSM1574322 SRP051602 SRS804880 GSM1574322 RNA-Seq TRANSCRIPTOMIC cDNA Sciatic nerves were freed from perineurial fibroblast layer and homogenized with a chilled pestle. Total RNA was subsequently extracted using Qiazol according to manufacturers description. The TruSeq RNA Sample Prep Kit v2 (Illumina, Inc.) was used in the succeeding steps. Briefly, total RNA samples (100-1000 ng) were depleted of ribosomal RNA using Ribo Zero Gold (Epicentre¨) and then reverse-transcribed into double-stranded cDNA. The cDNA samples were fragmented, end-repaired and polyadenylated before ligation of TruSeq adapters containing the index for multiplexing Fragments containing TruSeq adapters on both ends were selectively enriched with PCR. The quality and quantity of the enriched libraries were validated using Qubit¨ (1.0) Fluorometer and the Caliper GX LabChip¨ GX (Caliper Life Sciences, Inc.). The product is a smear with an average fragment size of approximately 260 bp. The libraries were normalized to 10nM in Tris-HCl 10 mM (pH 8.5) with 0.1% Tween 20. The TruSeq PE Cluster Kit v3-cBot-HS or TruSeq SR Cluster Kit v3-cBot-HS (Illumina, Inc.) was used for cluster generation using 10 pM of pooled normalized libraries on the cBOT. Sequencing were performed on the Illumina HiSeq 2000 paired end at 2 X101 bp or single end 100 bp using the TruSeq SBS Kit v3-HS (Illumina, Inc.) Illumina HiSeq 2000 GEO Sample GSM1574322 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1574322 gds 301574322 GEO Accession GSM1574322 SRX825338 GSM1574323 SRP051602 SRS804881 GSM1574323 RNA-Seq TRANSCRIPTOMIC cDNA Sciatic nerves were freed from perineurial fibroblast layer and homogenized with a chilled pestle. Total RNA was subsequently extracted using Qiazol according to manufacturers description. The TruSeq RNA Sample Prep Kit v2 (Illumina, Inc.) was used in the succeeding steps. Briefly, total RNA samples (100-1000 ng) were depleted of ribosomal RNA using Ribo Zero Gold (Epicentre¨) and then reverse-transcribed into double-stranded cDNA. The cDNA samples were fragmented, end-repaired and polyadenylated before ligation of TruSeq adapters containing the index for multiplexing Fragments containing TruSeq adapters on both ends were selectively enriched with PCR. The quality and quantity of the enriched libraries were validated using Qubit¨ (1.0) Fluorometer and the Caliper GX LabChip¨ GX (Caliper Life Sciences, Inc.). The product is a smear with an average fragment size of approximately 260 bp. The libraries were normalized to 10nM in Tris-HCl 10 mM (pH 8.5) with 0.1% Tween 20. The TruSeq PE Cluster Kit v3-cBot-HS or TruSeq SR Cluster Kit v3-cBot-HS (Illumina, Inc.) was used for cluster generation using 10 pM of pooled normalized libraries on the cBOT. Sequencing were performed on the Illumina HiSeq 2000 paired end at 2 X101 bp or single end 100 bp using the TruSeq SBS Kit v3-HS (Illumina, Inc.) Illumina HiSeq 2000 GEO Sample GSM1574323 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1574323 gds 301574323 GEO Accession GSM1574323 SRX825339 GSM1574324 SRP051602 SRS804882 GSM1574324 RNA-Seq TRANSCRIPTOMIC cDNA Sciatic nerves were freed from perineurial fibroblast layer and homogenized with a chilled pestle. Total RNA was subsequently extracted using Qiazol according to manufacturers description. The TruSeq RNA Sample Prep Kit v2 (Illumina, Inc.) was used in the succeeding steps. Briefly, total RNA samples (100-1000 ng) were depleted of ribosomal RNA using Ribo Zero Gold (Epicentre¨) and then reverse-transcribed into double-stranded cDNA. The cDNA samples were fragmented, end-repaired and polyadenylated before ligation of TruSeq adapters containing the index for multiplexing Fragments containing TruSeq adapters on both ends were selectively enriched with PCR. The quality and quantity of the enriched libraries were validated using Qubit¨ (1.0) Fluorometer and the Caliper GX LabChip¨ GX (Caliper Life Sciences, Inc.). The product is a smear with an average fragment size of approximately 260 bp. The libraries were normalized to 10nM in Tris-HCl 10 mM (pH 8.5) with 0.1% Tween 20. The TruSeq PE Cluster Kit v3-cBot-HS or TruSeq SR Cluster Kit v3-cBot-HS (Illumina, Inc.) was used for cluster generation using 10 pM of pooled normalized libraries on the cBOT. Sequencing were performed on the Illumina HiSeq 2000 paired end at 2 X101 bp or single end 100 bp using the TruSeq SBS Kit v3-HS (Illumina, Inc.) Illumina HiSeq 2000 GEO Sample GSM1574324 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1574324 gds 301574324 GEO Accession GSM1574324 SRX825340 GSM1574325 SRP051602 SRS804883 GSM1574325 RNA-Seq TRANSCRIPTOMIC cDNA Sciatic nerves were freed from perineurial fibroblast layer and homogenized with a chilled pestle. Total RNA was subsequently extracted using Qiazol according to manufacturers description. The TruSeq RNA Sample Prep Kit v2 (Illumina, Inc.) was used in the succeeding steps. Briefly, total RNA samples (100-1000 ng) were depleted of ribosomal RNA using Ribo Zero Gold (Epicentre¨) and then reverse-transcribed into double-stranded cDNA. The cDNA samples were fragmented, end-repaired and polyadenylated before ligation of TruSeq adapters containing the index for multiplexing Fragments containing TruSeq adapters on both ends were selectively enriched with PCR. The quality and quantity of the enriched libraries were validated using Qubit¨ (1.0) Fluorometer and the Caliper GX LabChip¨ GX (Caliper Life Sciences, Inc.). The product is a smear with an average fragment size of approximately 260 bp. The libraries were normalized to 10nM in Tris-HCl 10 mM (pH 8.5) with 0.1% Tween 20. The TruSeq PE Cluster Kit v3-cBot-HS or TruSeq SR Cluster Kit v3-cBot-HS (Illumina, Inc.) was used for cluster generation using 10 pM of pooled normalized libraries on the cBOT. Sequencing were performed on the Illumina HiSeq 2000 paired end at 2 X101 bp or single end 100 bp using the TruSeq SBS Kit v3-HS (Illumina, Inc.) Illumina HiSeq 2000 GEO Sample GSM1574325 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1574325 gds 301574325 GEO Accession GSM1574325 SRX825341 GSM1574326 SRP051602 SRS804884 GSM1574326 RNA-Seq TRANSCRIPTOMIC cDNA Sciatic nerves were freed from perineurial fibroblast layer and homogenized with a chilled pestle. Total RNA was subsequently extracted using Qiazol according to manufacturers description. The TruSeq RNA Sample Prep Kit v2 (Illumina, Inc.) was used in the succeeding steps. Briefly, total RNA samples (100-1000 ng) were depleted of ribosomal RNA using Ribo Zero Gold (Epicentre¨) and then reverse-transcribed into double-stranded cDNA. The cDNA samples were fragmented, end-repaired and polyadenylated before ligation of TruSeq adapters containing the index for multiplexing Fragments containing TruSeq adapters on both ends were selectively enriched with PCR. The quality and quantity of the enriched libraries were validated using Qubit¨ (1.0) Fluorometer and the Caliper GX LabChip¨ GX (Caliper Life Sciences, Inc.). The product is a smear with an average fragment size of approximately 260 bp. The libraries were normalized to 10nM in Tris-HCl 10 mM (pH 8.5) with 0.1% Tween 20. The TruSeq PE Cluster Kit v3-cBot-HS or TruSeq SR Cluster Kit v3-cBot-HS (Illumina, Inc.) was used for cluster generation using 10 pM of pooled normalized libraries on the cBOT. Sequencing were performed on the Illumina HiSeq 2000 paired end at 2 X101 bp or single end 100 bp using the TruSeq SBS Kit v3-HS (Illumina, Inc.) Illumina HiSeq 2000 GEO Sample GSM1574326 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1574326 gds 301574326 GEO Accession GSM1574326 SRX825342 GSM1574327 SRP051602 SRS804885 GSM1574327 RNA-Seq TRANSCRIPTOMIC cDNA Sciatic nerves were freed from perineurial fibroblast layer and homogenized with a chilled pestle. Total RNA was subsequently extracted using Qiazol according to manufacturers description. The TruSeq RNA Sample Prep Kit v2 (Illumina, Inc.) was used in the succeeding steps. Briefly, total RNA samples (100-1000 ng) were depleted of ribosomal RNA using Ribo Zero Gold (Epicentre¨) and then reverse-transcribed into double-stranded cDNA. The cDNA samples were fragmented, end-repaired and polyadenylated before ligation of TruSeq adapters containing the index for multiplexing Fragments containing TruSeq adapters on both ends were selectively enriched with PCR. The quality and quantity of the enriched libraries were validated using Qubit¨ (1.0) Fluorometer and the Caliper GX LabChip¨ GX (Caliper Life Sciences, Inc.). The product is a smear with an average fragment size of approximately 260 bp. The libraries were normalized to 10nM in Tris-HCl 10 mM (pH 8.5) with 0.1% Tween 20. The TruSeq PE Cluster Kit v3-cBot-HS or TruSeq SR Cluster Kit v3-cBot-HS (Illumina, Inc.) was used for cluster generation using 10 pM of pooled normalized libraries on the cBOT. Sequencing were performed on the Illumina HiSeq 2000 paired end at 2 X101 bp or single end 100 bp using the TruSeq SBS Kit v3-HS (Illumina, Inc.) Illumina HiSeq 2000 GEO Sample GSM1574327 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1574327 gds 301574327 GEO Accession GSM1574327 SRX825343 GSM1574328 SRP051602 SRS804886 GSM1574328 RNA-Seq TRANSCRIPTOMIC cDNA Sciatic nerves were freed from perineurial fibroblast layer and homogenized with a chilled pestle. Total RNA was subsequently extracted using Qiazol according to manufacturers description. The TruSeq RNA Sample Prep Kit v2 (Illumina, Inc.) was used in the succeeding steps. Briefly, total RNA samples (100-1000 ng) were depleted of ribosomal RNA using Ribo Zero Gold (Epicentre¨) and then reverse-transcribed into double-stranded cDNA. The cDNA samples were fragmented, end-repaired and polyadenylated before ligation of TruSeq adapters containing the index for multiplexing Fragments containing TruSeq adapters on both ends were selectively enriched with PCR. The quality and quantity of the enriched libraries were validated using Qubit¨ (1.0) Fluorometer and the Caliper GX LabChip¨ GX (Caliper Life Sciences, Inc.). The product is a smear with an average fragment size of approximately 260 bp. The libraries were normalized to 10nM in Tris-HCl 10 mM (pH 8.5) with 0.1% Tween 20. The TruSeq PE Cluster Kit v3-cBot-HS or TruSeq SR Cluster Kit v3-cBot-HS (Illumina, Inc.) was used for cluster generation using 10 pM of pooled normalized libraries on the cBOT. Sequencing were performed on the Illumina HiSeq 2000 paired end at 2 X101 bp or single end 100 bp using the TruSeq SBS Kit v3-HS (Illumina, Inc.) Illumina HiSeq 2000 GEO Sample GSM1574328 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1574328 gds 301574328 GEO Accession GSM1574328 SRX825344 GSM1574329 SRP051602 SRS804887 GSM1574329 RNA-Seq TRANSCRIPTOMIC cDNA Sciatic nerves were freed from perineurial fibroblast layer and homogenized with a chilled pestle. Total RNA was subsequently extracted using Qiazol according to manufacturers description. The TruSeq RNA Sample Prep Kit v2 (Illumina, Inc.) was used in the succeeding steps. Briefly, total RNA samples (100-1000 ng) were depleted of ribosomal RNA using Ribo Zero Gold (Epicentre¨) and then reverse-transcribed into double-stranded cDNA. The cDNA samples were fragmented, end-repaired and polyadenylated before ligation of TruSeq adapters containing the index for multiplexing Fragments containing TruSeq adapters on both ends were selectively enriched with PCR. The quality and quantity of the enriched libraries were validated using Qubit¨ (1.0) Fluorometer and the Caliper GX LabChip¨ GX (Caliper Life Sciences, Inc.). The product is a smear with an average fragment size of approximately 260 bp. The libraries were normalized to 10nM in Tris-HCl 10 mM (pH 8.5) with 0.1% Tween 20. The TruSeq PE Cluster Kit v3-cBot-HS or TruSeq SR Cluster Kit v3-cBot-HS (Illumina, Inc.) was used for cluster generation using 10 pM of pooled normalized libraries on the cBOT. Sequencing were performed on the Illumina HiSeq 2000 paired end at 2 X101 bp or single end 100 bp using the TruSeq SBS Kit v3-HS (Illumina, Inc.) Illumina HiSeq 2000 GEO Sample GSM1574329 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1574329 gds 301574329 GEO Accession GSM1574329 SRX825345 GSM1574330 SRP051602 SRS804888 GSM1574330 RNA-Seq TRANSCRIPTOMIC cDNA Sciatic nerves were freed from perineurial fibroblast layer and homogenized with a chilled pestle. Total RNA was subsequently extracted using Qiazol according to manufacturers description. The TruSeq RNA Sample Prep Kit v2 (Illumina, Inc.) was used in the succeeding steps. Briefly, total RNA samples (100-1000 ng) were depleted of ribosomal RNA using Ribo Zero Gold (Epicentre¨) and then reverse-transcribed into double-stranded cDNA. The cDNA samples were fragmented, end-repaired and polyadenylated before ligation of TruSeq adapters containing the index for multiplexing Fragments containing TruSeq adapters on both ends were selectively enriched with PCR. The quality and quantity of the enriched libraries were validated using Qubit¨ (1.0) Fluorometer and the Caliper GX LabChip¨ GX (Caliper Life Sciences, Inc.). The product is a smear with an average fragment size of approximately 260 bp. The libraries were normalized to 10nM in Tris-HCl 10 mM (pH 8.5) with 0.1% Tween 20. The TruSeq PE Cluster Kit v3-cBot-HS or TruSeq SR Cluster Kit v3-cBot-HS (Illumina, Inc.) was used for cluster generation using 10 pM of pooled normalized libraries on the cBOT. Sequencing were performed on the Illumina HiSeq 2000 paired end at 2 X101 bp or single end 100 bp using the TruSeq SBS Kit v3-HS (Illumina, Inc.) Illumina HiSeq 2000 GEO Sample GSM1574330 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1574330 gds 301574330 GEO Accession GSM1574330 SRX825346 GSM1574331 SRP051602 SRS804889 GSM1574331 RNA-Seq TRANSCRIPTOMIC cDNA Sciatic nerves were freed from perineurial fibroblast layer and homogenized with a chilled pestle. Total RNA was subsequently extracted using Qiazol according to manufacturers description. The TruSeq RNA Sample Prep Kit v2 (Illumina, Inc.) was used in the succeeding steps. Briefly, total RNA samples (100-1000 ng) were depleted of ribosomal RNA using Ribo Zero Gold (Epicentre¨) and then reverse-transcribed into double-stranded cDNA. The cDNA samples were fragmented, end-repaired and polyadenylated before ligation of TruSeq adapters containing the index for multiplexing Fragments containing TruSeq adapters on both ends were selectively enriched with PCR. The quality and quantity of the enriched libraries were validated using Qubit¨ (1.0) Fluorometer and the Caliper GX LabChip¨ GX (Caliper Life Sciences, Inc.). The product is a smear with an average fragment size of approximately 260 bp. The libraries were normalized to 10nM in Tris-HCl 10 mM (pH 8.5) with 0.1% Tween 20. The TruSeq PE Cluster Kit v3-cBot-HS or TruSeq SR Cluster Kit v3-cBot-HS (Illumina, Inc.) was used for cluster generation using 10 pM of pooled normalized libraries on the cBOT. Sequencing were performed on the Illumina HiSeq 2000 paired end at 2 X101 bp or single end 100 bp using the TruSeq SBS Kit v3-HS (Illumina, Inc.) Illumina HiSeq 2000 GEO Sample GSM1574331 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1574331 gds 301574331 GEO Accession GSM1574331 SRX825347 GSM1574332 SRP051602 SRS804890 GSM1574332 RNA-Seq TRANSCRIPTOMIC cDNA Sciatic nerves were freed from perineurial fibroblast layer and homogenized with a chilled pestle. Total RNA was subsequently extracted using Qiazol according to manufacturers description. The TruSeq RNA Sample Prep Kit v2 (Illumina, Inc.) was used in the succeeding steps. Briefly, total RNA samples (100-1000 ng) were depleted of ribosomal RNA using Ribo Zero Gold (Epicentre¨) and then reverse-transcribed into double-stranded cDNA. The cDNA samples were fragmented, end-repaired and polyadenylated before ligation of TruSeq adapters containing the index for multiplexing Fragments containing TruSeq adapters on both ends were selectively enriched with PCR. The quality and quantity of the enriched libraries were validated using Qubit¨ (1.0) Fluorometer and the Caliper GX LabChip¨ GX (Caliper Life Sciences, Inc.). The product is a smear with an average fragment size of approximately 260 bp. The libraries were normalized to 10nM in Tris-HCl 10 mM (pH 8.5) with 0.1% Tween 20. The TruSeq PE Cluster Kit v3-cBot-HS or TruSeq SR Cluster Kit v3-cBot-HS (Illumina, Inc.) was used for cluster generation using 10 pM of pooled normalized libraries on the cBOT. Sequencing were performed on the Illumina HiSeq 2000 paired end at 2 X101 bp or single end 100 bp using the TruSeq SBS Kit v3-HS (Illumina, Inc.) Illumina HiSeq 2000 GEO Sample GSM1574332 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1574332 gds 301574332 GEO Accession GSM1574332 SRX825348 GSM1574333 SRP051602 SRS804891 GSM1574333 RNA-Seq TRANSCRIPTOMIC cDNA Sciatic nerves were freed from perineurial fibroblast layer and homogenized with a chilled pestle. Total RNA was subsequently extracted using Qiazol according to manufacturers description. The TruSeq RNA Sample Prep Kit v2 (Illumina, Inc.) was used in the succeeding steps. Briefly, total RNA samples (100-1000 ng) were depleted of ribosomal RNA using Ribo Zero Gold (Epicentre¨) and then reverse-transcribed into double-stranded cDNA. The cDNA samples were fragmented, end-repaired and polyadenylated before ligation of TruSeq adapters containing the index for multiplexing Fragments containing TruSeq adapters on both ends were selectively enriched with PCR. The quality and quantity of the enriched libraries were validated using Qubit¨ (1.0) Fluorometer and the Caliper GX LabChip¨ GX (Caliper Life Sciences, Inc.). The product is a smear with an average fragment size of approximately 260 bp. The libraries were normalized to 10nM in Tris-HCl 10 mM (pH 8.5) with 0.1% Tween 20. The TruSeq PE Cluster Kit v3-cBot-HS or TruSeq SR Cluster Kit v3-cBot-HS (Illumina, Inc.) was used for cluster generation using 10 pM of pooled normalized libraries on the cBOT. Sequencing were performed on the Illumina HiSeq 2000 paired end at 2 X101 bp or single end 100 bp using the TruSeq SBS Kit v3-HS (Illumina, Inc.) Illumina HiSeq 2000 GEO Sample GSM1574333 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1574333 gds 301574333 GEO Accession GSM1574333